Methocarbamol

Product NDC

43063-860

11-digit product format

430630860

Labeler code

43063

Product ID

43063-860_77f6049d-d620-c483-e053-2991aa0ac829

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA090200

Marketing category

ANDA

Marketing start

2013-03-20

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