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"70771-1152-4" National Drug Code (NDC)
Finasteride 10 BLISTER PACK in 1 CARTON (70771-1152-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Zydus Lifesciences Limited)
NDC Code
70771-1152-4
Package Description
10 BLISTER PACK in 1 CARTON (70771-1152-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
70771-1152
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20171205
Marketing Category Name
ANDA
Application Number
ANDA078900
Manufacturer
Zydus Lifesciences Limited
Substance Name
FINASTERIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70771-1152-4