Ciprofloxacin

Product NDC
63629-2313
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA208921
Marketing category
ANDA
Substance
CIPROFLOXACIN HYDROCHLORIDE
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-2313-1100 TABLET, COATED in 1 BOTTLE (63629-2313-1) 2021-02-170000-00-00NoCurrent