Methocarbamol

Product NDC

50436-4026

11-digit product format

504364026

Labeler code

50436

Product ID

50436-4026_5d8c9708-c98d-4045-868a-ba6cf61ba872

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

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