Cyclobenzaprine Hydrochloride

Product NDC

68071-1998

11-digit product format

680711998

Labeler code

68071

Product ID

68071-1998_6249fa66-0947-a6e4-e053-2991aa0a5b5e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA078048

Marketing category

ANDA

Marketing start

2014-07-31

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