Cyclobenzaprine Hydrochloride

Product NDC

70518-0390

11-digit product format

705180390

Labeler code

70518

Product ID

70518-0390_842bf78d-8105-121c-e053-2a91aa0a87f4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA090478

Marketing category

ANDA

Marketing start

2017-04-04

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

2020-12-31

Current FDA listing

Historical FDA.report record