Carisoprodol

Product NDC

50436-3435

11-digit product format

504363435

Labeler code

50436

Product ID

50436-3435_de5fbc65-b5ae-4717-ab51-eabcc2ddad76

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carisoprodol

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA040755

Marketing category

ANDA

Marketing start

2007-02-27

Marketing end

0000-00-00

Substance

CARISOPRODOL

Active strength

350 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

DEA schedule

CIV

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record