NDC 68788-9178

Prednisone

Prednisone

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

Product ID68788-9178_502c39a5-658d-4dd1-87b0-26a838efbd4f
NDC68788-9178
Product TypeHuman Prescription Drug
Proprietary NamePrednisone
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2011-07-21
Marketing CategoryANDA / ANDA
Application NumberANDA040256
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NamePREDNISONE
Active Ingredient Strength10 mg/1
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 68788-9178-1

10 TABLET in 1 BOTTLE, DISPENSING (68788-9178-1)
Marketing Start Date2011-07-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9178-6 [68788917806]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-3 [68788917803]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-8 [68788917808]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-2 [68788917802]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-7 [68788917807]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-1 [68788917801]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-5 [68788917805]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-9 [68788917809]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

NDC 68788-9178-4 [68788917804]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-07-21

Drug Details

Active Ingredients

IngredientStrength
PREDNISONE10 mg/1

OpenFDA Data

SPL SET ID:a1769552-f230-40e0-8f05-5b3b356437b6
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.