Baclofen

Product NDC
70518-4378
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Baclofen
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA215885
Marketing category
ANDA
Substance
BACLOFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70518-4378-090 TABLET in 1 BOTTLE, PLASTIC (70518-4378-0) 2025-07-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Baclofen Tablets, USP Rx onlyREMEDYREPACK INC.2025-07-01HUMAN PRESCRIPTION DRUG LABEL1