Cyclobenzaprine Hydrochloride

Product NDC

55154-5571

11-digit product format

551545571

Labeler code

55154

Product ID

55154-5571_5729bb8d-04cf-454c-96df-f4a71b1b2bb5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cyclobenzaprine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA073144

Marketing category

ANDA

Marketing start

2011-07-15

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