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"70934-880-21" National Drug Code (NDC)
Prednisone 21 TABLET in 1 BOTTLE, PLASTIC (70934-880-21)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)
NDC Code
70934-880-21
Package Description
21 TABLET in 1 BOTTLE, PLASTIC (70934-880-21)
Product NDC
70934-880
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisone
Non-Proprietary Name
Prednisone
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20210802
End Marketing Date
20240531
Marketing Category Name
ANDA
Application Number
ANDA080292
Manufacturer
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance Name
PREDNISONE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70934-880-21