Cyclobenzaprine Hydrochloride

Product NDC

57237-191

11-digit product format

572370191

Labeler code

57237

Product ID

57237-191_52408032-5f3e-4157-a271-e910ac514102

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Citron Pharma LLC

Application

ANDA078643

Marketing category

ANDA

Marketing start

2008-09-26

Marketing end

0000-00-00

Substance

CYCLOBENZAPRINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record