Methocarbamol

Product NDC

50090-3391

11-digit product format

500903391

Labeler code

50090

Product ID

50090-3391_dd71dbe9-c598-4cdd-af6c-d56226d8cb13

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA200958

Marketing category

ANDA

Marketing start

2015-07-13

Marketing end

0000-00-00

Substance

METHOCARBAMOL

Active strength

750 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record