Cyclobenzaprine Hydrochloride

Product NDC

55700-311

11-digit product format

557000311

Labeler code

55700

Product ID

55700-311_0931e598-ab92-4534-8769-cdf3845ea329

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclobenzaprine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

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

2019-12-31

Current FDA listing

Historical FDA.report record