Cyclobenzaprine Hydrochloride

Product NDC

50090-2761

11-digit product format

500902761

Labeler code

50090

Product ID

50090-2761_6ba7ee55-8a34-48f6-a965-71c735512125

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

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