Cyclobenzaprine Hydrochloride

Product NDC

68071-3149

11-digit product format

680713149

Labeler code

68071

Product ID

68071-3149_4a29a31f-ec1d-4603-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA090478

Marketing category

ANDA

Marketing start

2016-07-22

Marketing end

0000-00-00

Substance

CYCLOBENZAPRINE HYDROCHLORIDE

Active strength

5 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