NDC 51655-320

Prednisone

Prednisone

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

Product ID51655-320_abd6c038-2c14-4d9a-88a4-b823a8874b28
NDC51655-320
Product TypeHuman Prescription Drug
Proprietary NamePrednisone
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-05-01
Marketing CategoryANDA / ANDA
Application NumberANDA088832
Labeler NameNorthwind Pharmaceuticals
Substance NamePREDNISONE
Active Ingredient Strength20 mg/201
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 51655-320-21

21 TABLET in 1 BOTTLE, DISPENSING (51655-320-21)
Marketing Start Date2014-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51655-320-30 [51655032030]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA088832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-04-29
Inactivation Date2020-01-31

NDC 51655-320-18 [51655032018]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA088832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-04-29
Inactivation Date2020-01-31

NDC 51655-320-54 [51655032054]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA088832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-01-22
Inactivation Date2020-01-31

NDC 51655-320-21 [51655032021]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA088832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-04-29
Inactivation Date2020-01-31

NDC 51655-320-53 [51655032053]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA088832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-01-22
Inactivation Date2020-01-31

NDC 51655-320-20 [51655032020]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA088832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-05-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PREDNISONE20 mg/201

OpenFDA Data

SPL SET ID:2a994060-a358-4835-892b-0eb1f0806eb0
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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