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"55111-172-78" National Drug Code (NDC)
Finasteride 10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)
(Dr. Reddy's Laboratories Limited)
NDC Code
55111-172-78
Package Description
10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)
Product NDC
55111-172
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070228
Marketing Category Name
ANDA
Application Number
ANDA076437
Manufacturer
Dr. Reddy's Laboratories 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/55111-172-78