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"69097-112-05" National Drug Code (NDC)
Finasteride 90 TABLET in 1 BOTTLE (69097-112-05)
(Cipla USA Inc.)
NDC Code
69097-112-05
Package Description
90 TABLET in 1 BOTTLE (69097-112-05)
Product NDC
69097-112
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20141120
Marketing Category Name
ANDA
Application Number
ANDA077335
Manufacturer
Cipla USA Inc.
Substance Name
FINASTERIDE
Strength
1
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/69097-112-05