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"47335-715-18" National Drug Code (NDC)
Finasteride 1000 TABLET, FILM COATED in 1 BOTTLE (47335-715-18)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
47335-715-18
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (47335-715-18)
Product NDC
47335-715
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20221125
Marketing Category Name
ANDA
Application Number
ANDA090507
Manufacturer
Sun Pharmaceutical Industries, Inc.
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/47335-715-18