NDC 70934-471

PREDNISONE

Prednisone

PREDNISONE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The primary component is Prednisone.

Product ID70934-471_9cb38da1-ec4b-3926-e053-2995a90a1e45
NDC70934-471
Product TypeHuman Prescription Drug
Proprietary NamePREDNISONE
Generic NamePrednisone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-12-09
Marketing CategoryANDA / ANDA
Application NumberANDA210525
Labeler NameDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NamePREDNISONE
Active Ingredient Strength20 mg/1
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 70934-471-10

10 TABLET in 1 BOTTLE, PLASTIC (70934-471-10)
Marketing Start Date2019-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70934-471-10 [70934047110]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA210525
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-30

NDC 70934-471-30 [70934047130]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA210525
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-09

NDC 70934-471-21 [70934047121]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA210525
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-09

NDC 70934-471-15 [70934047115]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA210525
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-30

NDC 70934-471-20 [70934047120]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA210525
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-09

NDC 70934-471-12 [70934047112]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA210525
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-01-09

NDC 70934-471-40 [70934047140]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA210525
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-01-09

Drug Details

Active Ingredients

IngredientStrength
PREDNISONE20 mg/1

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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