Methocarbamol

Product NDC
67046-1147
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Coupler LLC
Application
ANDA090200
Marketing category
ANDA
Substance
METHOCARBAMOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
67046-1147-330 TABLET in 1 BLISTER PACK (67046-1147-3) 2025-01-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol Tablets USP Rx OnlyCoupler LLC2025-01-30HUMAN PRESCRIPTION DRUG LABEL1