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"52125-996-03" National Drug Code (NDC)
Prednisone 20 TABLET in 1 BOTTLE (52125-996-03)
(REMEDYREPACK INC.)
NDC Code
52125-996-03
Package Description
20 TABLET in 1 BOTTLE (52125-996-03)
Product NDC
52125-996
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisone
Non-Proprietary Name
Prednisone
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140801
Marketing Category Name
ANDA
Application Number
ANDA083677
Manufacturer
REMEDYREPACK INC.
Substance Name
PREDNISONE
Strength
20
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-996-03