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"50436-1720-5" National Drug Code (NDC)
Prednisone 21 TABLET in 1 BOTTLE (50436-1720-5)
(Unit Dose Services)
NDC Code
50436-1720-5
Package Description
21 TABLET in 1 BOTTLE (50436-1720-5)
Product NDC
50436-1720
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisone
Non-Proprietary Name
Prednisone
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20010829
Marketing Category Name
ANDA
Application Number
ANDA040362
Manufacturer
Unit Dose Services
Substance Name
PREDNISONE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50436-1720-5