Methocarbamol

Product NDC

68788-9076

11-digit product format

687889076

Labeler code

68788

Product ID

68788-9076_d811c4cd-7f31-419c-bc75-7414007f8ac1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA040489

Marketing category

ANDA

Marketing start

2010-08-06

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