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"16571-884-10" National Drug Code (NDC)
Allopurinol 1000 TABLET in 1 BOTTLE (16571-884-10)
(Rising Pharma Holdings, Inc.)
NDC Code
16571-884-10
Package Description
1000 TABLET in 1 BOTTLE (16571-884-10)
Product NDC
16571-884
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Allopurinol
Non-Proprietary Name
Allopurinol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230921
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA016084
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
ALLOPURINOL
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-884-10