FDA.report

prednisone

Product NDC
71205-818
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
prednisone
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA213386
Marketing category
ANDA
Substance
PREDNISONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71205-818-055 TABLET in 1 BOTTLE, PLASTIC (71205-818-05) 2023-07-03NoHistorical
71205-818-066 TABLET in 1 BOTTLE, PLASTIC (71205-818-06) 2023-07-03NoHistorical
71205-818-077 TABLET in 1 BOTTLE, PLASTIC (71205-818-07) 2023-07-03NoHistorical
71205-818-1010 TABLET in 1 BOTTLE, PLASTIC (71205-818-10) 2023-07-03NoHistorical
71205-818-1212 TABLET in 1 BOTTLE, PLASTIC (71205-818-12) 2023-07-03NoHistorical
71205-818-1414 TABLET in 1 BOTTLE, PLASTIC (71205-818-14) 2023-07-03NoHistorical
71205-818-1515 TABLET in 1 BOTTLE, PLASTIC (71205-818-15) 2023-07-03NoHistorical
71205-818-2020 TABLET in 1 BOTTLE, PLASTIC (71205-818-20) 2023-07-03NoHistorical
71205-818-2121 TABLET in 1 BOTTLE, PLASTIC (71205-818-21) 2023-07-03NoHistorical
71205-818-2424 TABLET in 1 BOTTLE, PLASTIC (71205-818-24) 2023-07-03NoHistorical
71205-818-2828 TABLET in 1 BOTTLE, PLASTIC (71205-818-28) 2023-07-03NoHistorical
71205-818-3030 TABLET in 1 BOTTLE, PLASTIC (71205-818-30) 2023-07-03NoHistorical
71205-818-4040 TABLET in 1 BOTTLE, PLASTIC (71205-818-40) 2023-07-03NoHistorical
71205-818-4242 TABLET in 1 BOTTLE, PLASTIC (71205-818-42) 2023-07-03NoHistorical
71205-818-6060 TABLET in 1 BOTTLE, PLASTIC (71205-818-60) 2023-07-03NoHistorical
71205-818-9090 TABLET in 1 BOTTLE, PLASTIC (71205-818-90) 2023-07-03NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PredniSONE Tablets, USP (10 mg) Rx onlyProficient Rx LP2023-07-01HUMAN PRESCRIPTION DRUG LABEL1