NDC 63187-066

Prednisone

Prednisone

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

Product ID63187-066_748ccf30-eb1f-4667-8cc7-3a87a8aba359
NDC63187-066
Product TypeHuman Prescription Drug
Proprietary NamePrednisone
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2002-07-12
Marketing CategoryANDA / ANDA
Application NumberANDA040256
Labeler NameProficient Rx LP
Substance NamePREDNISONE
Active Ingredient Strength5 mg/1
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 63187-066-05

5 TABLET in 1 BOTTLE (63187-066-05)
Marketing Start Date2014-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63187-066-30 [63187006630]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-12 [63187006612]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-05 [63187006605]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-06 [63187006606]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-40 [63187006640]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-24 [63187006624]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-20 [63187006620]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-21 [63187006621]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-42 [63187006642]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-08 [63187006608]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-09 [63187006609]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

NDC 63187-066-15 [63187006615]

Prednisone TABLET
Marketing CategoryANDA
Application NumberANDA040256
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-01

Drug Details

Active Ingredients

IngredientStrength
PREDNISONE5 mg/1

OpenFDA Data

SPL SET ID:7d52bf53-76e3-4826-a12b-b16a8560bafc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312617
  • 198145
  • 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.