U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C13H21NO3.ClH
Molecular Weight 275.772
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVALBUTEROL HYDROCHLORIDE

SMILES

Cl.CC(C)(C)NC[C@H](O)C1=CC(CO)=C(O)C=C1

InChI

InChIKey=OWNWYCOLFIFTLK-YDALLXLXSA-N
InChI=1S/C13H21NO3.ClH/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15;/h4-6,12,14-17H,7-8H2,1-3H3;1H/t12-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C13H21NO3
Molecular Weight 239.3107
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Levalbuterol is the (R)-enantiomer of the drug substance racemic albuterol (salbutamol). Binding studies have demonstrated that (R)-albuterol binds to the beta2-adrenergic receptor with a high affinity, whereas (S)-albuterol binds with 100-fold less affinity than (R)-albuterol. Other evaluations have suggested that (R)-albuterol possesses the bronchodilatory, bronchoprotective, and ciliary-stimulatory properties of racemic albuterol, while (S)-albuterol does not contribute beneficially to the therapeutic effects of the racemate and was originally assumed to be inert. Xopenex (levalbuterol HCl) Inhalation Solution is indicated for the treatment or prevention of bronchospasm in adults, adolescents, and children 6 years of age and older with reversible obstructive airway disease.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
236.0 nM [Kd]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
XOPENEX

Approved Use

XOPENEX (levalbuterol HCl) Inhalation Solution Concentrate is indicated for the treatment or prevention of bronchospasm in adults, adolescents, and children 6 years of age and older with reversible obstructive airway disease.

Launch Date

1999
Primary
XOPENEX

Approved Use

XOPENEX (levalbuterol HCl) Inhalation Solution Concentrate is indicated for the treatment or prevention of bronchospasm in adults, adolescents, and children 6 years of age and older with reversible obstructive airway disease.

Launch Date

1999
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
1.1 ng/mL
1.25 mg single, respiratory
dose: 1.25 mg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
4.5 ng/mL
1.25 mg 4 times / 2 hours multiple, respiratory
dose: 1.25 mg
route of administration: Respiratory
experiment type: MULTIPLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
0.303 ng/mL
0.31 mg single, respiratory
dose: 0.31 mg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
0.521 ng/mL
0.63 mg single, respiratory
dose: 0.63 mg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
199 pg/mL
90 μg single, respiratory
dose: 90 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
238 pg/mL
180 μg single, respiratory
dose: 180 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
163 pg/mL
90 μg single, respiratory
dose: 90 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
238 pg/mL
180 μg single, respiratory
dose: 180 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
3.3 ng × h/mL
1.25 mg single, respiratory
dose: 1.25 mg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
17.4 ng × h/mL
1.25 mg 4 times / 2 hours multiple, respiratory
dose: 1.25 mg
route of administration: Respiratory
experiment type: MULTIPLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
1.36 ng × h/mL
0.31 mg single, respiratory
dose: 0.31 mg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
2.55 ng × h/mL
0.63 mg single, respiratory
dose: 0.63 mg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
695 pg × h/mL
90 μg single, respiratory
dose: 90 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
798 pg × h/mL
180 μg single, respiratory
dose: 180 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
579 pg × h/mL
90 μg single, respiratory
dose: 90 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
828 pg × h/mL
180 μg single, respiratory
dose: 180 μg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
3.3 h
1.25 mg single, respiratory
dose: 1.25 mg
route of administration: Respiratory
experiment type: SINGLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
4 h
1.25 mg 4 times / 2 hours multiple, respiratory
dose: 1.25 mg
route of administration: Respiratory
experiment type: MULTIPLE
co-administered:
LEVALBUTEROL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
90.55%
LEVALBUTEROL plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
90 ug 1 times / day steady, respiratory
Recommended
Dose: 90 ug, 1 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 1 times / day
Sources:
unhealthy, 4 - 11 years
Health Status: unhealthy
Age Group: 4 - 11 years
Sex: M+F
Sources:
Disc. AE: Asthma...
AEs leading to
discontinuation/dose reduction:
Asthma (1 patient)
Sources:
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Disc. AE: Bronchitis, Dyspnea...
Other AEs: Apparent life threatening event, Bronchitis...
AEs leading to
discontinuation/dose reduction:
Bronchitis (45 patients)
Dyspnea (45 patients)
Lung disorder (45 patients)
Other AEs:
Apparent life threatening event (18 patients)
Bronchitis (131 patient)
Dyspnea (131 patient)
Lung disorder (131 patient)
Tachycardia (67 patients)
Palpitation (67 patients)
Chest pain (67 patients)
Arrhythmia (67 patients)
Hypertension (67 patients)
Dyspepsia (67 patients)
Nausea (67 patients)
Leg cramps (67 patients)
Sources:
AEs

AEs

AESignificanceDosePopulation
Asthma 1 patient
Disc. AE
90 ug 1 times / day steady, respiratory
Recommended
Dose: 90 ug, 1 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 1 times / day
Sources:
unhealthy, 4 - 11 years
Health Status: unhealthy
Age Group: 4 - 11 years
Sex: M+F
Sources:
Bronchitis 131 patient
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Dyspnea 131 patient
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Lung disorder 131 patient
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Apparent life threatening event 18 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Bronchitis 45 patients
Disc. AE
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Dyspnea 45 patients
Disc. AE
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Lung disorder 45 patients
Disc. AE
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Arrhythmia 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Chest pain 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Dyspepsia 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Hypertension 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Leg cramps 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Nausea 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Palpitation 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Tachycardia 67 patients
90 ug 4 times / day steady, respiratory
Studied dose
Dose: 90 ug, 4 times / day
Route: respiratory
Route: steady
Dose: 90 ug, 4 times / day
Sources:
unhealthy, > 12 years
Health Status: unhealthy
Age Group: > 12 years
Sex: M+F
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Comparison of racemic albuterol and levalbuterol for treatment of acute asthma.
2003-12
Mirror images: is levalbuterol the fairest of them all?
2003-12
Effect of surface covering of lactose carrier particles on dry powder inhalation properties of salbutamol sulfate.
2003-12
Influence of mechanical activation on the physical stability of salbutamol sulphate.
2003-11
Changes in heart rate associated with nebulized racemic albuterol and levalbuterol in intensive care patients.
2003-10-01
Effect of humidity on aerosolization of micronized drugs.
2003-10
A meta-analysis of randomized controlled trials evaluating the efficacy of epinephrine for the treatment of acute viral bronchiolitis.
2003-10
Albuterol aerosol delivered via metered-dose inhaler to intubated pediatric models of 3 ages, with 4 spacer designs.
2003-10
Retrospective comparison of nebulized levalbuterol and albuterol for adverse events in patients with acute airflow obstruction.
2003-09-17
Effects of carriers and storage of formulation on the lung deposition of a hydrophobic and hydrophilic drug from a DPI.
2003-09-16
Investigation of the physical properties of spray-dried stabilised lysozyme particles.
2003-09
Management of the acute exacerbation of asthma.
2003-09
Levalbuterol is not more cost-effective than albuterol for COPD.
2003-09
Levalbuterol vs racemic albuterol: science or drug company propaganda?
2003-09
An evaluation of nebulized levalbuterol in stable COPD.
2003-09
Urgent adenotonsillectomy: an analysis of risk factors associated with postoperative respiratory morbidity.
2003-09
Albuterol improves response to levodopa and increases skeletal muscle mass in patients with fluctuating Parkinson disease.
2003-08-05
Self-hypnosis for anxiety associated with severe asthma: a case report.
2003-07-22
Characterisation and deposition studies of engineered lactose crystals with potential for use as a carrier for aerosolised salbutamol sulfate from dry powder inhalers.
2003-07
Levalbuterol is as effective as racemic albuterol in lowering serum potassium.
2003-07
Three useful bromimetric methods for the determination of salbutamol sulfate.
2003-07
Planar gamma scintigraphy--points to consider when quantifying pulmonary dry powder aerosol deposition.
2003-06-04
Levalbuterol: pharmacologic properties and use in the treatment of pediatric and adult asthma.
2003-06
Levalbuterol toxicity: no reason to be jittery.
2003-06
(R,S)-salbutamol plasma concentrations in severe asthma.
2003-06
The influence of carrier and drug morphology on drug delivery from dry powder formulations.
2003-05-12
Immobilization of fine particles on lactose carrier by precision coating and its effect on the performance of dry powder formulations.
2003-05
Investigation into the effect of humidity on drug-drug interactions using the atomic force microscope.
2003-04
A system for the production and delivery of monodisperse salbutamol aerosols to the lungs.
2003-03-26
Characterisation of surface modified salbutamol sulphate-alkylpolyglycoside microparticles prepared by spray drying.
2003-03-06
Characterization of particle-interactions by atomic force microscopy: effect of contact area.
2003-03
The effect of mechanical processing on surface stability of pharmaceutical powders: visualization by atomic force microscopy.
2003-03
Managing outpatient asthma exacerbations.
2003-03
Single-isomer levalbuterol: a review of the acute data.
2003-03
Influence of physico-chemical carrier properties on the in vitro aerosol deposition from interactive mixtures.
2003-02-18
Prospective observational cohort safety study to monitor the introduction of a non-CFC formulation of salbutamol with HFA134a in England.
2003-02
Effect of aerosolized albuterol sulfate on resting energy expenditure determined by use of open-flow indirect calorimetry in horses with recurrent airway obstruction.
2003-02
Launois-Bensaude syndrome in a female with type 2 diabetes.
2003-02
Planar gamma scintigraphy--points to consider when quantifying pulmonary dry powder aerosol deposition.
2003-01-30
Metabolism of salbutamol differs between asthmatic patients and healthy volunteers.
2003-01
Levalbuterol compared to racemic albuterol: efficacy and outcomes in patients hospitalized with COPD or asthma.
2003-01
Preparation of dry powder inhalation by surface treatment of lactose carrier particles.
2003-01
Novolizer: a multidose dry powder inhaler.
2003
Investigation of processing parameters of spray freezing into liquid to prepare polyethylene glycol polymeric particles for drug delivery.
2003
Salbutamol sulfate suppositories: influence of formulation on physical parameters and stability.
2003
Application of the chiral acyl anion equivalent, trans-1,3-dithiane 1,3-dioxide, to an asymmetric synthesis of (R)-salbutamol.
2002-11-29
In vitro evaluation of the release of albuterol sulfate from polymer gels: effect of fatty acids on drug transport across biological membranes.
2002-11
The effect of heliox-driven bronchodilator aerosol therapy on pulmonary function tests in patients with asthma.
2002-10
Comparison of innovator and generic salbutamol inhalers: a double-blind randomized study of efficacy and tolerance.
2002
Apparent ELISA detection times for albuterol after administration with the torpex equine inhaler device.
2002
Patents

Patents

Sample Use Guides

Children 6–11 years old: The recommended dosage of Xopenex (levalbuterol HCl) Inhalation Solution for patients 6–11 years old is 0.31 mg administered three times a day, by nebulization. Routine dosing should not exceed 0.63 mg three times a day. Adults and Adolescents ≥12 years old: The recommended starting dosage of Xopenex (levalbuterol HCl) Inhalation Solution for patients 12 years of age and older is 0.63 mg administered three times a day, every 6 to 8 hours, by nebulization.
Route of Administration: Respiratory
In Vitro Use Guide
Curator's Comment: Levalbuterol inhibits cell growth by activating the cAMP/PKA pathway and inhibiting PI-3 kinase, NF-kappaB and Rb protein expression
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:12:02 GMT 2025
Edited
by admin
on Mon Mar 31 18:12:02 GMT 2025
Record UNII
WDQ1526QJM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVALBUTEROL HYDROCHLORIDE
ORANGE BOOK   USAN   USP   USP-RS  
USAN  
Official Name English
LEVOSALBUTAMOL HYDROCHLORIDE
MART.   WHO-DD  
Preferred Name English
LEVALBUTEROL HYDROCHLORIDE [ORANGE BOOK]
Common Name English
LEVALBUTEROL HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
NSC-759255
Code English
LEVALBUTEROL HYDROCHLORIDE [USP-RS]
Common Name English
ALBUTEROL HYDROCHLORIDE, R-
Common Name English
ALBUTEROL (R)-FORM HYDROCHLORIDE [MI]
Common Name English
Levosalbutamol hydrochloride [WHO-DD]
Common Name English
LEVOSALBUTAMOL HYDROCHLORIDE [MART.]
Common Name English
LEVALBUTEROL HCL
Common Name English
(R)-.ALPHA.(SUP 1)-((TERT-BUTYLAMINO)METHYL)-4-HYDROXY-M-XYLENE-.ALPHA.,.ALPHA.'-DIOL HYDROCHLORIDE
Common Name English
XOPENEX
Brand Name English
LEVALBUTEROL HYDROCHLORIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
Code System Code Type Description
EVMPD
SUB02915MIG
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
ChEMBL
CHEMBL1002
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
RXCUI
237160
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY RxNorm
CAS
50293-90-8
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
PUBCHEM
123601
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
NCI_THESAURUS
C47580
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
MERCK INDEX
m1480
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY Merck Index
SMS_ID
100000086147
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
DRUG BANK
DBSALT001453
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
FDA UNII
WDQ1526QJM
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
USAN
JJ-19
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
NSC
759255
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID20198296
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
DAILYMED
WDQ1526QJM
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
RS_ITEM_NUM
1358784
Created by admin on Mon Mar 31 18:12:02 GMT 2025 , Edited by admin on Mon Mar 31 18:12:02 GMT 2025
PRIMARY
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