Methocarbamol

Product NDC

68788-9768

11-digit product format

687889768

Labeler code

68788

Product ID

68788-9768_ac11d429-88ee-4266-b87d-8ecd1ce480c0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA086988

Marketing category

ANDA

Marketing start

2015-08-20

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

2020-12-31

Current FDA listing

Historical FDA.report record