Cyclobenzaprine Hydrochloride

Product NDC

55289-567

11-digit product format

552890567

Labeler code

55289

Product ID

55289-567_3e08af89-92f3-4b9e-807d-77cd2b00bd38

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA078218

Marketing category

ANDA

Marketing start

2010-02-18

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