Cyclobenzaprine Hydrochloride

Product NDC

55154-7884

11-digit product format

551547884

Labeler code

55154

Product ID

55154-7884_78de71e2-c7a1-46bd-8d7f-e8a645d7370c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA071611

Marketing category

ANDA

Marketing start

1988-02-29

Marketing end

2020-07-31

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