NDC 70518-0242

Prednisone

Prednisone

Prednisone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Prednisone.

Product ID70518-0242_8359e178-ba20-c0b8-e053-2991aa0add18
NDC70518-0242
Product TypeHuman Prescription Drug
Proprietary NamePrednisone
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-02-20
Marketing CategoryANDA / ANDA
Application NumberANDA040362
Labeler NameREMEDYREPACK INC.
Substance NamePREDNISONE
Active Ingredient Strength20 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70518-0242-0

16 TABLET in 1 BOTTLE, PLASTIC (70518-0242-0)
Marketing Start Date2017-02-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0242-0 [70518024200]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040362
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-20
Marketing End Date2018-02-22

NDC 70518-0242-1 [70518024201]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040362
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-25
Marketing End Date2020-03-31

NDC 70518-0242-2 [70518024202]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040362
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-21
Marketing End Date2019-03-20

NDC 70518-0242-4 [70518024204]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040362
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-10-03
Marketing End Date2019-10-04

NDC 70518-0242-5 [70518024205]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040362
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-01
Marketing End Date2020-03-31

NDC 70518-0242-3 [70518024203]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040362
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-25
Marketing End Date2020-03-31

Drug Details

Active Ingredients

IngredientStrength
PREDNISONE20 mg/1

OpenFDA Data

SPL SET ID:4d2320e3-9fbe-435e-a2b0-71dbe3e558c8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312615
  • 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

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