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"61919-108-20" National Drug Code (NDC)
Prednisone 20 TABLET in 1 BOTTLE (61919-108-20)
(Direct_Rx)
NDC Code
61919-108-20
Package Description
20 TABLET in 1 BOTTLE (61919-108-20)
Product NDC
61919-108
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisone
Non-Proprietary Name
Prednisone
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190807
Marketing Category Name
ANDA
Application Number
ANDA040362
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/61919-108-20