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"70377-071-12" National Drug Code (NDC)
Everolimus 6 BLISTER PACK in 1 CARTON (70377-071-12) / 10 TABLET in 1 BLISTER PACK
(Biocon Pharma Inc.)
NDC Code
70377-071-12
Package Description
6 BLISTER PACK in 1 CARTON (70377-071-12) / 10 TABLET in 1 BLISTER PACK
Product NDC
70377-071
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Everolimus
Non-Proprietary Name
Everolimus
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20250602
Marketing Category Name
ANDA
Application Number
ANDA216140
Manufacturer
Biocon Pharma Inc.
Substance Name
EVEROLIMUS
Strength
.75
Strength Unit
mg/1
Pharmacy Classes
Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70377-071-12