Carisoprodol

Product NDC

63739-049

11-digit product format

637390049

Labeler code

63739

Product ID

63739-049_800858d7-2fcc-46c1-99a1-3093ecbb2eaf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carisoprodol

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA040245

Marketing category

ANDA

Marketing start

1997-09-08

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record