Baclofen

Product NDC
70771-1868
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Baclofen
Dosage form
TABLET
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA211659
Marketing category
ANDA
Substance
BACLOFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70771-1868-1100 TABLET in 1 BOTTLE (70771-1868-1) 2024-06-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
BACLOFEN TABLETS USP Rx onlyZydus Lifesciences Limited2024-08-12HUMAN PRESCRIPTION DRUG LABEL8