Methocarbamol

Product NDC
63629-9288
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040489
Marketing category
ANDA
Substance
METHOCARBAMOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-9288-1100 TABLET in 1 BOTTLE (63629-9288-1) 2022-06-06NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol Tablets, USP 500 mg Methocarbamol Tablets, USP 750 mg Rx OnlyBryant Ranch Prepack2024-04-04HUMAN PRESCRIPTION DRUG LABEL102