Cyclobenzaprine Hydrochloride

Product NDC

66267-064

11-digit product format

662670064

Labeler code

66267

Product ID

66267-064_3d966e77-9332-4051-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA090478

Marketing category

ANDA

Marketing start

2012-04-02

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

2020-12-31

Current FDA listing

Historical FDA.report record