cyclobenzaprine hydrochloride

Product NDC

0179-0189

11-digit product format

001790189

Labeler code

0179

Product ID

0179-0189_7ba9d445-42d6-5fc8-e053-2991aa0a0d3f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cyclobenzaprine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

ANDA077563

Marketing category

ANDA

Marketing start

2015-11-10

Marketing end

2019-12-31

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

0000-00-00

Current FDA listing

Historical FDA.report record