Cyclobenzaprine Hydrochloride

Product NDC
71610-428
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
cyclobenzaprine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA077797
Marketing category
ANDA
Substance
CYCLOBENZAPRINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71610-428-4545 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-428-45) 2020-05-15NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CYCLOBENZAPRINE HYDROCHLORIDE TABLETS, USP Rx onlyAphena Pharma Solutions - Tennessee, LLC2020-05-27HUMAN PRESCRIPTION DRUG LABEL1