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"72189-430-21" National Drug Code (NDC)
Prednisone 21 TABLET in 1 BOTTLE (72189-430-21)
(Direct_Rx)
NDC Code
72189-430-21
Package Description
21 TABLET in 1 BOTTLE (72189-430-21)
Product NDC
72189-430
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisone
Non-Proprietary Name
Prednisone
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230303
Marketing Category Name
ANDA
Application Number
ANDA208412
Manufacturer
Direct_Rx
Substance Name
PREDNISONE
Strength
20
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/72189-430-21