Cyclobenzaprine Hydrochloride

Product NDC

68645-518

11-digit product format

686450518

Labeler code

68645

Product ID

68645-518_0a8d5f09-e039-4f7d-b095-e1e50d05552e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

ANDA090478

Marketing category

ANDA

Marketing start

2016-07-22

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