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Search results for amphotericin root_codes_comments in Code Comments (approximate match)
Status:
US Previously Marketed
First approved in 1957
Class:
POLYMER
Status:
First approved in 1951
Class:
POLYMER
Status:
US Previously Marketed
Source:
Paraformaldehyde U.S.P.
(1921)
Source URL:
First marketed in 1921
Source:
Paraformaldehyde U.S.P.
Source URL:
Class:
POLYMER
Status:
Possibly Marketed Outside US
Source:
M020
(2018)
Source URL:
First approved in 2018
Source:
M020
Source URL:
Class:
POLYMER
Status:
Possibly Marketed Outside US
Source:
ANDA203695
(2017)
Source URL:
First approved in 2017
Source:
ANDA203695
Source URL:
Class:
POLYMER
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(2010)
Source URL:
First approved in 2010
Source:
21 CFR 352
Source URL:
Class:
POLYMER
Status:
Possibly Marketed Outside US
Source:
Antiseptic Rinse by Meijer
(2006)
Source URL:
First approved in 1994
Source:
ANDA074558
Source URL:
Class:
POLYMER
Status:
Possibly Marketed Outside US
Source:
MSM (MoSaengMo) by Handock Cosmetics Inc
(2011)
Source URL:
First approved in 1990
Source:
21 CFR 333A
Source URL:
Class:
POLYMER
Status:
Possibly Marketed Outside US
First approved in 1984
Source:
Hemocyte F by US Pharmaceutical Corporation
Source URL:
Class:
POLYMER
Hypromellose is a semisynthetic, inert, viscoelastic methyl and hydroxypropyl mixed ether of cellulose used as eye drops, as well as an excipient and controlled-delivery component in oral medicaments, found in a variety of commercial products. Hypromellose is considered an inert substance as it has no direct pharmacological activity. The viscosity promoting properties of hypromellose prolong the retention time and improve adhesion of synthetic tears to the cornea and conjunctiva. As a result, the tear film breakdown time is prolonged and/or the tear film stability is enhanced. A stable tear film protects the cornea from dryness Hypromellose is the most commonly used in hydrophilic matrix fabrication. Hypromellose provides the release of a drug in a controlled manner, effectively increasing the duration of release of a drug to prolong its therapeutic effect.
Status:
Possibly Marketed Outside US
Source:
Therabloat by Norden
Source URL:
First approved in 1963
Source:
NADA038281
Source URL:
Class:
POLYMER
