Tiopronin

Product NDC
0480-7824
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tiopronin
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Teva Pharmaceuticals, Inc.
Application
ANDA216456
Marketing category
ANDA
Substance
TIOPRONIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0480-7824-9890 TABLET, DELAYED RELEASE in 1 BOTTLE (0480-7824-98) 2024-10-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
TioproninTeva Pharmaceuticals, Inc.2024-06-28HUMAN PRESCRIPTION DRUG LABEL4