Methocarbamol

Product NDC
50090-3587
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol Tablets
Dosage form
TABLET, COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA209312
Marketing category
ANDA
Substance
METHOCARBAMOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-3587-090 TABLET, COATED in 1 BOTTLE (50090-3587-0) 2018-09-26NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol Tablets Rx OnlyA-S Medication Solutions2025-11-26HUMAN PRESCRIPTION DRUG LABEL1