Cyclobenzaprine Hydrochloride

Product NDC

0615-7528

11-digit product format

006157528

Labeler code

0615

Product ID

0615-7528_3cdef1be-879c-49a7-817e-e4fdc171168c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cyclobenzaprine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA077797

Marketing category

ANDA

Marketing start

2007-02-28

Marketing end

0000-00-00

Substance

CYCLOBENZAPRINE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record