prednisone

Product NDC
71205-729
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PREDNISONE
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA208412
Marketing category
ANDA
Substance
PREDNISONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71205-729-1010 TABLET in 1 BOTTLE, PLASTIC (71205-729-10) 2022-12-12NoHistorical
71205-729-1414 TABLET in 1 BOTTLE, PLASTIC (71205-729-14) 2022-12-12NoHistorical
71205-729-1818 TABLET in 1 BOTTLE, PLASTIC (71205-729-18) 2024-02-15NoHistorical
71205-729-2020 TABLET in 1 BOTTLE, PLASTIC (71205-729-20) 2022-12-12NoHistorical
71205-729-2121 TABLET in 1 BOTTLE, PLASTIC (71205-729-21) 2022-12-12NoHistorical
71205-729-2828 TABLET in 1 BOTTLE, PLASTIC (71205-729-28) 2024-10-31NoHistorical
71205-729-3030 TABLET in 1 BOTTLE, PLASTIC (71205-729-30) 2022-12-12NoHistorical
71205-729-4040 TABLET in 1 BOTTLE, PLASTIC (71205-729-40) 2023-10-25NoHistorical
71205-729-4242 TABLET in 1 BOTTLE, PLASTIC (71205-729-42) 2025-04-21NoHistorical
71205-729-6060 TABLET in 1 BOTTLE, PLASTIC (71205-729-60) 2022-12-12NoHistorical
71205-729-6363 TABLET in 1 BOTTLE, PLASTIC (71205-729-63) 2022-12-12NoHistorical
71205-729-9090 TABLET in 1 BOTTLE, PLASTIC (71205-729-90) 2022-12-12NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PredniSONE Tablets USP Rx onlyProficient Rx LP2025-04-01HUMAN PRESCRIPTION DRUG LABEL5