Methocarbamol

Product NDC

50090-0176

11-digit product format

500900176

Labeler code

50090

Product ID

50090-0176_d71f3668-4f14-405c-87fe-5bb3c344b33e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA085159

Marketing category

ANDA

Marketing start

2000-01-01

Marketing end

0000-00-00

Substance

METHOCARBAMOL

Active strength

500 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