NDC 50090-0095

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 ID50090-0095_a6b85aac-9f8d-4794-b76e-60e5fc8e6f39
NDC50090-0095
Product TypeHuman Prescription Drug
Proprietary NamePrednisone
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-08-03
Marketing CategoryANDA / ANDA
Application NumberANDA080292
Labeler NameA-S Medication Solutions
Substance NamePREDNISONE
Active Ingredient Strength5 mg/1
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50090-0095-7

60 TABLET in 1 BOTTLE (50090-0095-7)
Marketing Start Date2014-11-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-0095-0 [50090009500]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2019-09-30

NDC 50090-0095-7 [50090009507]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2019-09-30

NDC 50090-0095-4 [50090009504]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2019-09-30

NDC 50090-0095-1 [50090009501]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2019-02-28

NDC 50090-0095-3 [50090009503]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2019-09-30

Drug Details

Active Ingredients

IngredientStrength
PREDNISONE5 mg/1

OpenFDA Data

SPL SET ID:d2d21782-3cee-43cf-ad45-d2a64d1386d5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312615
  • 312617

    • Pharmacological Class

    • Corticosteroid [EPC]
    • Corticosteroid Hormone Receptor Agonists [MoA]

    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.