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"71921-178-20" National Drug Code (NDC)
Abiraterone Acetate 120 TABLET in 1 BOTTLE (71921-178-20)
(Florida Pharmaceutical Products, LLC.)
NDC Code
71921-178-20
Package Description
120 TABLET in 1 BOTTLE (71921-178-20)
Product NDC
71921-178
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Abiraterone Acetate
Non-Proprietary Name
Abiraterone Acetate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220815
Marketing Category Name
ANDA
Application Number
ANDA212462
Manufacturer
Florida Pharmaceutical Products, LLC.
Substance Name
ABIRATERONE ACETATE
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Cytochrome P450 17A1 Inhibitor [EPC], Cytochrome P450 17A1 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71921-178-20