NDC 49999-028

Prednisone

Prednisone

Prednisone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Lake Erie Medical Dba Quality Care Products Llc. The primary component is Prednisone.

Product ID49999-028_0d8b6719-907e-49bb-ac00-c53f0b069377
NDC49999-028
Product TypeHuman Prescription Drug
Proprietary NamePrednisone
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-08-11
Marketing CategoryANDA / ANDA
Application NumberANDA040256
Labeler NameLake Erie medical DBA Quality Care Products LLC
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 49999-028-40

40 TABLET in 1 BOTTLE, PLASTIC (49999-028-40)
Marketing Start Date2010-08-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49999-028-65 [49999002865]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11
Marketing End Date2014-06-01

NDC 49999-028-60 [49999002860]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11

NDC 49999-028-20 [49999002820]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11
Marketing End Date2014-06-01

NDC 49999-028-48 [49999002848]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11
Marketing End Date2014-06-01

NDC 49999-028-12 [49999002812]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11
Marketing End Date2014-06-01

NDC 49999-028-14 [49999002814]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11
Marketing End Date2014-06-01

NDC 49999-028-40 [49999002840]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11

NDC 49999-028-15 [49999002815]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11
Marketing End Date2014-06-01

NDC 49999-028-21 [49999002821]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-09-05

NDC 49999-028-30 [49999002830]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-11
Marketing End Date2014-06-01

Drug Details

Active Ingredients

IngredientStrength
PREDNISONE10 mg/1

OpenFDA Data

SPL SET ID:8d3cb614-20c1-4a6d-9e89-22785f78c56e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198145
  • Pharmacological Class

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