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"0093-4232-01" National Drug Code (NDC)
Bumetanide 100 TABLET in 1 BOTTLE (0093-4232-01)
(Teva Pharmaceuticals USA Inc)
NDC Code
0093-4232-01
Package Description
100 TABLET in 1 BOTTLE (0093-4232-01)
Product NDC
0093-4232
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bumetanide
Non-Proprietary Name
Bumetanide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071016
Marketing Category Name
ANDA
Application Number
ANDA074225
Manufacturer
Teva Pharmaceuticals USA Inc
Substance Name
BUMETANIDE
Strength
.5
Strength Unit
mg/1
Pharmacy Classes
Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-4232-01