Cyclobenzaprine Hydrochloride

Product NDC

55700-459

11-digit product format

557000459

Labeler code

55700

Product ID

55700-459_729f751e-f360-451a-b8a7-a6a01252db9a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA090478

Marketing category

ANDA

Marketing start

2016-07-22

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record