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Details

Stereochemistry ACHIRAL
Molecular Formula C15H19N5.C7H6O2
Molecular Weight 391.4662
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIZATRIPTAN BENZOATE

SMILES

OC(=O)C1=CC=CC=C1.CN(C)CCC2=CNC3=CC=C(CN4C=NC=N4)C=C23

InChI

InChIKey=JPRXYLQNJJVCMZ-UHFFFAOYSA-N
InChI=1S/C15H19N5.C7H6O2/c1-19(2)6-5-13-8-17-15-4-3-12(7-14(13)15)9-20-11-16-10-18-20;8-7(9)6-4-2-1-3-5-6/h3-4,7-8,10-11,17H,5-6,9H2,1-2H3;1-5H,(H,8,9)

HIDE SMILES / InChI

Molecular Formula C15H19N5
Molecular Weight 269.3449
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H6O2
Molecular Weight 122.1213
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.drugbank.ca/drugs/DB00953 | https://www.drugs.com/pro/rizatriptan-orally-disintegrating-tablets.html | http://reference.medscape.com/drug/maxalt-maxalt-mlt-rizatriptan-343033 | https://www.ncbi.nlm.nih.gov/pubmed/9357514

Rizatriptan (trade name Maxalt) is a 5-HT1 receptor agonist of the triptan class of drugs developed by Merck & Co. for the treatment of migraine headaches. Rizatriptan (trade name Maxalt) is a 5-HT1 receptor agonist of the triptan class of drugs developed by Merck & Co. for the treatment of migraine headaches. Rizatriptan acts as an agonist at serotonin 5-HT1B and 5-HT1D receptors. Rizatriptan binds with high affinity to human cloned 5-HT1B/1D receptors. Rizatriptan benzoate presumably exerts its therapeutic effects in the treatment of a migraine headache by binding to 5-HT1B/1D receptors located on intracranial blood vessels and sensory nerves of the trigeminal system. Rizatriptan is completely absorbed following oral administration. The mean oral absolute bioavailability of the rizatriptan benzoate tablet is about 45%, and mean peak plasma concentrations are reached in approximately 1-1.5 hours. The presence of a migraine headache did not appear to affect the absorption or pharmacokinetics of rizatriptan. Food has no significant effect on the bioavailability of rizatriptan but delays the time to reach peak concentration by an hour. The primary route of rizatriptan metabolism is via oxidative deamination by monoamine oxidase-A (MAO-A) to the indole acetic acid metabolite, which is not active at the 5-HT1B/1D receptor. N-mono-desmethyl-rizatriptan, a metabolite with activity similar to that of parent compound at the 5-HT1B/1D receptor, is formed to a minor degree. Plasma concentrations of N-mono-desmethyl-rizatriptan are approximately 14% of those of parent compound, and it is eliminated at a similar rate. Other minor metabolites, the N-oxide, the 6-hydroxy compound, and the sulfate conjugate of the 6-hydroxy metabolite are not active at the 5-HT1B/1D receptor.

Originator

Curator's Comment: # Merck Sharp and Dohme Ltd.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
10.1 nM [Ki]
3.0 nM [EC50]
140.0 nM [Ki]
7.9 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
MAXALT

Approved Use

MAXALT is indicated for the acute treatment of migraine attacks with or without aura in adults. MAXALT is not intended for the prophylactic therapy of migraine or for use in the management of hemiplegic or basilar migraine (see CONTRAINDICATIONS). Safety and effectiveness of MAXALT have not been established for cluster headache, which is present in an older, predominantly male population.

Launch Date

1998
Primary
MAXALT

Approved Use

MAXALT is indicated for the acute treatment of migraine attacks with or without aura in adults. MAXALT is not intended for the prophylactic therapy of migraine or for use in the management of hemiplegic or basilar migraine (see CONTRAINDICATIONS). Safety and effectiveness of MAXALT have not been established for cluster headache, which is present in an older, predominantly male population.

Launch Date

1998
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
44.8 ng/mL
15 mg single, oral
dose: 15 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
6.2 ng/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
54 ng/mL
15 mg single, oral
dose: 15 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
6.1 ng/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
12.7 ng/mL
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
13.2 ng/mL
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
27.29 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
28.6 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
32.1 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
127 ng × h/mL
15 mg single, oral
dose: 15 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
16 ng × h/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
161 ng × h/mL
15 mg single, oral
dose: 15 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
19 ng × h/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
33 ng × h/mL
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
42 ng × h/mL
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
68 ng × h/mL
4 mg single, intravenous
dose: 4 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
69.88 ng × h/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
72 ng × h/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
84 ng × h/mL
4 mg single, intravenous
dose: 4 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
97 ng × h/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
2.4 h
15 mg single, oral
dose: 15 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
2.1 h
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
2.4 h
15 mg single, oral
dose: 15 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
2.2 h
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
2.2 h
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
2.4 h
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
2.9 h
4 mg single, intravenous
dose: 4 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
2.4 h
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
2.4 h
4 mg single, intravenous
dose: 4 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
2.6 h
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIZATRIPTAN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
10 mg single, oral
Recommended
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 17 years
n = 1
Health Status: unhealthy
Age Group: 17 years
Sex: F
Population Size: 1
Sources:
Other AEs: Jaundice...
Other AEs:
Jaundice
Sources:
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25 years
n = 2
Health Status: unhealthy
Age Group: 25 years
Sex: M
Population Size: 2
Sources:
Other AEs: Syncope, Incontinence...
Other AEs:
Syncope (1 patient)
Incontinence (1 patient)
Sources:
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25-29 years
n = 2
Health Status: unhealthy
Age Group: 25-29 years
Sex: M+F
Population Size: 2
Sources:
Other AEs: Dizziness...
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 29 years
n = 2
Health Status: unhealthy
Age Group: 29 years
Sex: F
Population Size: 2
Sources:
Other AEs: Vomiting, Bradycardia...
Other AEs:
Vomiting (1 patient)
Bradycardia (1 patient)
Sources:
10 mg 2 times / day multiple, oral
Recommended
Dose: 10 mg, 2 times / day
Route: oral
Route: multiple
Dose: 10 mg, 2 times / day
Co-administed with::
tacrolimus(8.5 mg/day; oral)
Sources:
unhealthy, 43 years
n = 1
Health Status: unhealthy
Age Group: 43 years
Sex: M
Population Size: 1
Sources:
Disc. AE: Transient ischemic attack...
AEs leading to
discontinuation/dose reduction:
Transient ischemic attack
Sources:
AEs

AEs

AESignificanceDosePopulation
Jaundice
10 mg single, oral
Recommended
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 17 years
n = 1
Health Status: unhealthy
Age Group: 17 years
Sex: F
Population Size: 1
Sources:
Incontinence 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25 years
n = 2
Health Status: unhealthy
Age Group: 25 years
Sex: M
Population Size: 2
Sources:
Syncope 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25 years
n = 2
Health Status: unhealthy
Age Group: 25 years
Sex: M
Population Size: 2
Sources:
Dizziness 2 patients
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25-29 years
n = 2
Health Status: unhealthy
Age Group: 25-29 years
Sex: M+F
Population Size: 2
Sources:
Bradycardia 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 29 years
n = 2
Health Status: unhealthy
Age Group: 29 years
Sex: F
Population Size: 2
Sources:
Vomiting 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 29 years
n = 2
Health Status: unhealthy
Age Group: 29 years
Sex: F
Population Size: 2
Sources:
Transient ischemic attack Disc. AE
10 mg 2 times / day multiple, oral
Recommended
Dose: 10 mg, 2 times / day
Route: oral
Route: multiple
Dose: 10 mg, 2 times / day
Co-administed with::
tacrolimus(8.5 mg/day; oral)
Sources:
unhealthy, 43 years
n = 1
Health Status: unhealthy
Age Group: 43 years
Sex: M
Population Size: 1
Sources:
PubMed

PubMed

TitleDatePubMed
Characterisation of the 5-HT receptor binding profile of eletriptan and kinetics of [3H]eletriptan binding at human 5-HT1B and 5-HT1D receptors.
1999 Mar 5
Rizatriptan: pharmacological differences from sumatriptan and clinical results.
2001
Sumatriptan: pharmacological basis and clinical results.
2001
Comparison of preference for rizatriptan 10-mg wafer versus sumatriptan 50-mg tablet in migraine.
2001
[Current topics: expectation for new triptans].
2001 Apr 10
Rizatriptan wafer--sublingual vs. placebo at the onset of acute migraine.
2001 Feb
Influence of beta-adrenoceptor antagonists on the pharmacokinetics of rizatriptan, a 5-HT1B/1D agonist: differential effects of propranolol, nadolol and metoprolol.
2001 Jul
Establishing a standard of speed for assessing the efficacy of the serotonin(1B/1D) agonists (triptans).
2001 Jul
Acute treatment of migraine and the role of triptans.
2001 Mar
Evidence-based migraine therapy.
2001 Nov
[Cost effectiveness of treatment with triptanes in Spain].
2001 Nov 16-30
Pharmacokinetics of rizatriptan in healthy elderly subjects.
2001 Oct
Effect of rizatriptan and other triptans on the nausea symptom of migraine: a post hoc analysis.
2001 Sep
What matters is not the differences between triptans, but the differences between patients.
2001 Sep
Restoring migraine sufferers' ability to function normally: a comparison of rizatriptan and other triptans in randomized trials.
2002
Rizatriptan: an update of its use in the management of migraine.
2002
[Satisfaction and recovery of normal activity with rizatriptan 10 mg. Results from the open, prospective, observational 4M study].
2002 Dec
Rizatriptan 5 mg for the acute treatment of migraine in adolescents: a randomized, double-blind, placebo-controlled study.
2002 Jan
[Treatment of migraine in patients with hypertension and ischemic heart disease].
2002 Jan 20
Mechanisms of action of the 5-HT1B/1D receptor agonists.
2002 Jul
The effect of rizatriptan, ergotamine, and their combination on human peripheral arteries: a double-blind, placebo-controlled, crossover study in normal subjects.
2002 Jul
Gateways to Clinical Trials. June 2002.
2002 Jun
Rizatriptan combined with rofecoxib vs. rizatriptan for the acute treatment of migraine: an open label pilot study.
2002 May
CNS effects of sumatriptan and rizatriptan in healthy female volunteers.
2002 May
Triptans (serotonin, 5-HT1B/1D agonists) in migraine: detailed results and methods of a meta-analysis of 53 trials.
2002 Oct
[New onset headache. Which patients should be sent for CT imaging?].
2002 Oct 24
Comparison of rizatriptan and other triptans on stringent measures of efficacy.
2002 Sep 10
Coprescription of triptans with potentially interacting medications: a cohort study involving 240,268 patients.
2003 Jan
[New therapeutic recommendations for severe migraine. High beginning dosage rather than slow dosage increase].
2003 Jan 30
Safety profile of the triptans.
2003 Mar
Real-world experiences in migraine therapy with rizatriptan.
2003 Mar
[Highly selective beginning. Associated symptoms and side effects in retrospect].
2003 May 26
Cost-effectiveness of almotriptan and rizatriptan in the treatment of acute migraine.
2003 Nov
Triptans for treatment of acute pediatric migraine: a systematic literature review.
2003 Nov
Investigation of the effects of naratriptan, rizatriptan, and sumatriptan on jugular venous oxygen saturation in anesthetized pigs: implications for their mechanism of acute antimigraine action.
2003 Oct
Naratriptan for the treatment of acute migraine: meta-analysis of randomised controlled trials.
2004 Feb
Evaluating triptan usage.
2004 Feb
Productivity cost benefit to employers of treating migraine with rizatriptan: a specific worksite analysis and model.
2004 Jan
Defeating migraine pain with triptans: a race against the development of cutaneous allodynia.
2004 Jan
Neuronal expression and regulation of CGRP promoter activity following viral gene transfer into cultured trigeminal ganglia neurons.
2004 Jan 30
Fast onset medications through thermally generated aerosols.
2004 May
Patents

Sample Use Guides

5-10 mg PO at onset of symptoms; repeat dose after 2 hours if necessary; not to exceed 30 mg/24 hr
Route of Administration: Oral
In Vitro Use Guide
Rizatriptan intrinsic efficacy, expressed as percent of the maximal 5-HT response, was measured in cloned human 5-HT1D and 5-HT1B receptors stably expressed in CHO cells using agonist-induced [35S]GTPγS binding. In this assay, interaction of the agonist-occupied receptor with the G-protein results in dissociation of GDP from the G-protein R-subunit and the binding of a molecule of GTP. Under normal conditions the R-subunit dissociates from the âγ-subunits and, following modulation of its effector, intrinsic R-subunit GTPase hydrolyzes the GTP to GDP. Because [35S]GTPγS is resistant to this GTPase, it accumulates in the membrane and it can be measured by virtue of its radiolabel
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:30:39 GMT 2023
Edited
by admin
on Fri Dec 15 16:30:39 GMT 2023
Record UNII
WR978S7QHH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RIZATRIPTAN BENZOATE
JAN   MART.   MI   ORANGE BOOK   USAN   USP-RS   VANDF   WHO-DD  
USAN  
Official Name English
NSC-758919
Code English
RIZATRIPTAN BENZOATE [USP-RS]
Common Name English
RIZATRIPTAN BENZOATE [EP MONOGRAPH]
Common Name English
1H-INDOLE-3-ETHANAMINE, N,N-DIMETHYL-5-(1H-1,2,4-TRIAZOL-1-YLMETHYL)-, MONOBENZOATE
Systematic Name English
RIZATRIPTAN BENZOATE [VANDF]
Common Name English
RIZATRIPTAN BENZOATE [USP MONOGRAPH]
Common Name English
RIZATRIPTAN BENZOATE [USAN]
Common Name English
MAXALT
Brand Name English
Rizatriptan benzoate [WHO-DD]
Common Name English
RIZATRIPTAN BENZOATE [ORANGE BOOK]
Common Name English
RIZATRIPTAN BENZOATE [JAN]
Common Name English
RIZAFILM
Brand Name English
RIZATRIPTAN BENZOATE [MART.]
Common Name English
MK-0462
Code English
3-[2-(Dimethylamino)ethyl]-5-(1H-1,2,4-triazol-1-ylmethyl)indole monobenzoate
Systematic Name English
RIZATRIPTAN BENZOATE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47794
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
Code System Code Type Description
CAS
145202-66-0
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID20162937
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
RXCUI
237082
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY RxNorm
USAN
HH-46
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
ChEMBL
CHEMBL905
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
PUBCHEM
77997
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
EVMPD
SUB04258MIG
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
NCI_THESAURUS
C47708
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
FDA UNII
WR978S7QHH
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
DAILYMED
WR978S7QHH
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
SMS_ID
100000090268
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
RS_ITEM_NUM
1604880
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
MERCK INDEX
m9640
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB00953
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
NSC
758919
Created by admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 2023
PRIMARY
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