Ciprofloxacin

Product NDC
60760-676
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin
Dosage form
TABLET, COATED
Route
ORAL
Labeler
St. Mary's Medical Park Pharmacy
Application
ANDA208921
Marketing category
ANDA
Substance
CIPROFLOXACIN HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60760-676-1010 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-10) 2021-05-28NoHistorical
60760-676-2020 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-20) 2021-05-21NoHistorical

Related DailyMed Labels