Methocarbamol

Product NDC

50090-0174

11-digit product format

500900174

Labeler code

50090

Product ID

50090-0174_af010477-03ff-40f3-ba95-9fb1bfcaa6bb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040489

Marketing category

ANDA

Marketing start

2003-01-29

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