Cyclobenzaprine Hydrochloride

Product NDC

51079-644

11-digit product format

510790644

Labeler code

51079

Product ID

51079-644_9aee2cfb-93c7-0835-e053-2a95a90a4249

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cyclobenzaprine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA073144

Marketing category

ANDA

Marketing start

1997-08-25

Marketing end

2020-06-30

Substance

CYCLOBENZAPRINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record