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"69097-859-07" National Drug Code (NDC)
Terbinafine 100 TABLET in 1 BOTTLE (69097-859-07)
(Cipla USA Inc.)
NDC Code
69097-859-07
Package Description
100 TABLET in 1 BOTTLE (69097-859-07)
Product NDC
69097-859
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Terbinafine
Non-Proprietary Name
Terbinafine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160627
Marketing Category Name
ANDA
Application Number
ANDA077533
Manufacturer
Cipla USA Inc.
Substance Name
TERBINAFINE HYDROCHLORIDE
Strength
250
Strength Unit
1/1
Pharmacy Classes
Allylamine Antifungal [EPC], Allylamine [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69097-859-07