Cyclobenzaprine Hydrochloride

Product NDC

50090-3329

11-digit product format

500903329

Labeler code

50090

Product ID

50090-3329_25299972-9a5f-47d9-8ed8-ace6895be955

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA071611

Marketing category

ANDA

Marketing start

1989-05-03

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