Carisoprodol

Product NDC

70518-0704

11-digit product format

705180704

Labeler code

70518

Product ID

70518-0704_8b4ee5b0-7590-4f55-e053-2995a90ab4aa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carisoprodol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA040245

Marketing category

ANDA

Marketing start

2017-08-21

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