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"67877-668-38" National Drug Code (NDC)
Febuxostat 10 BLISTER PACK in 1 CARTON (67877-668-38) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Ascend Laboratories, LLC)
NDC Code
67877-668-38
Package Description
10 BLISTER PACK in 1 CARTON (67877-668-38) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
67877-668
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Febuxostat
Non-Proprietary Name
Febuxostat
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20211208
Marketing Category Name
ANDA
Application Number
ANDA212924
Manufacturer
Ascend Laboratories, LLC
Substance Name
FEBUXOSTAT
Strength
40
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/67877-668-38