Methocarbamol

Product NDC
50090-4162
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA208507
Marketing category
ANDA
Substance
METHOCARBAMOL
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-4162-090 TABLET, FILM COATED in 1 BOTTLE (50090-4162-0) 2019-02-260000-00-00NoCurrent