cyclobenzaprine hydrochloride

Product NDC

0179-0057

11-digit product format

001790057

Labeler code

0179

Product ID

0179-0057_7b9a5b1c-afc4-12cc-e053-2a91aa0a07be

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

2010-03-02

Marketing end

2020-02-29

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