Baclofen

Product NDC
60687-815
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Baclofen
Dosage form
TABLET
Route
ORAL
Labeler
American Health Packaging
Application
ANDA211659
Marketing category
ANDA
Substance
BACLOFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60687-815-01100 BLISTER PACK in 1 CARTON (60687-815-01) / 1 TABLET in 1 BLISTER PACK (60687-815-11) 2024-05-26NoHistorical
60687-815-6550 BLISTER PACK in 1 CARTON (60687-815-65) / 1 TABLET in 1 BLISTER PACK (60687-815-11) 2025-08-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Baclofen Tablets, USP Rx Only 8480465/0525FAmerican Health Packaging2025-08-04HUMAN PRESCRIPTION DRUG LABEL4