prednisone

Product NDC
60760-790
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PREDNISONE
Dosage form
TABLET
Route
ORAL
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Application
ANDA208412
Marketing category
ANDA
Substance
PREDNISONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60760-790-1212 TABLET in 1 BOTTLE, PLASTIC (60760-790-12) 2022-07-20NoHistorical
60760-790-2121 TABLET in 1 BOTTLE, PLASTIC (60760-790-21) 2022-07-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PredniSONE Tablets USP Rx onlyST. MARY'S MEDICAL PARK PHARMACY2022-07-20HUMAN PRESCRIPTION DRUG LABEL1