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"0093-1125-89" National Drug Code (NDC)
Abiraterone Acetate 120 TABLET, FILM COATED in 1 BOTTLE (0093-1125-89)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-1125-89
Package Description
120 TABLET, FILM COATED in 1 BOTTLE (0093-1125-89)
Product NDC
0093-1125
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Abiraterone Acetate
Non-Proprietary Name
Abiraterone Acetate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20181121
Marketing Category Name
ANDA
Application Number
ANDA208432
Manufacturer
Teva Pharmaceuticals USA, Inc.
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/0093-1125-89