NDC 50090-0097

Prednisone

Prednisone

Prednisone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Prednisone.

Product ID50090-0097_34cc5e60-b3dd-4034-b714-fb0d39ee94c3
NDC50090-0097
Product TypeHuman Prescription Drug
Proprietary NamePrednisone
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2002-07-12
Marketing CategoryANDA / ANDA
Application NumberANDA040256
Labeler NameA-S Medication Solutions
Substance NamePREDNISONE
Active Ingredient Strength10 mg/1
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 50090-0097-0

10 TABLET in 1 BOTTLE (50090-0097-0)
Marketing Start Date2016-06-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-0097-0 [50090009700]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-21
Marketing End Date2018-04-30

NDC 50090-0097-2 [50090009702]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2018-01-31

NDC 50090-0097-4 [50090009704]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2018-01-31

NDC 50090-0097-5 [50090009705]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2018-04-30

NDC 50090-0097-7 [50090009707]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2017-07-31

NDC 50090-0097-8 [50090009708]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2018-01-31

NDC 50090-0097-1 [50090009701]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2018-01-31

Drug Details

NDC Crossover Matching brand name "Prednisone" or generic name "Prednisone"

NDCBrand NameGeneric Name
0054-0017PredniSONEPredniSONE
0054-0018PredniSONEPredniSONE
0054-0019PredniSONEPredniSONE
0054-3722PredniSONEPredniSONE
0054-4728PredniSONEPredniSONE
0054-4741PredniSONEPredniSONE
68071-1777PrednisonePrednisone
68071-1779PrednisonePrednisone
68071-3143PrednisonePrednisone
68071-4319PrednisonePrednisone
68071-4546PrednisonePrednisone
68071-4685PrednisonePrednisone
68071-4691PrednisonePrednisone
68071-4491PrednisonePrednisone
68151-0820PredniSONEPredniSONE
0440-8167PrednisonePrednisone
0440-8165PrednisonePrednisone
0463-6155PredniSONEPredniSONE
68258-3013PrednisonePrednisone
0463-6141PredniSONEPredniSONE
68387-240PrednisonePrednisone
68387-241PrednisonePrednisone
68788-6440PrednisonePrednisone
68788-6414PrednisonePrednisone
68788-7281PrednisonePrednisone
68788-7372PrednisonePrednisone
68788-9309PrednisonePrednisone
68788-9178PrednisonePrednisone
68788-9551PrednisonePrednisone
0054-4742PredniSONEPredniSONE
0054-8739PredniSONEPredniSONE
0054-8724PredniSONEPredniSONE
0054-8740PredniSONEPredniSONE
70518-0305PrednisonePrednisone
70518-0307PrednisonePrednisone
70518-0205PrednisonePrednisone
70518-0306PredniSONEPredniSONE
70518-0242PrednisonePrednisone
70518-0073PrednisonePrednisone
70518-0473PrednisonePrednisone
70518-0632PrednisonePrednisone
70518-1116PredniSONEPredniSONE
70518-1167PrednisonePrednisone
70518-0948PrednisonePrednisone
70518-0800PrednisonePrednisone
70518-1105PredniSONEPredniSONE
70518-1119PrednisonePrednisone
70518-1120PrednisonePrednisone
0591-5442PrednisonePrednisone
70518-1854PrednisonePrednisone
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.