Cyclobenzaprine Hydrochloride

Product NDC

60760-417

11-digit product format

607600417

Labeler code

60760

Product ID

60760-417_7a7fdefb-fb02-0153-e053-2991aa0a183e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cyclobenzaprine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

St. Mary's Medical Park Pharmacy

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record