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"0172-2083-80" National Drug Code (NDC)
Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (0172-2083-80)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0172-2083-80
Package Description
1000 TABLET in 1 BOTTLE (0172-2083-80)
Product NDC
0172-2083
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydrochlorothiazide
Non-Proprietary Name
Hydrochlorothiazide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
19730112
Marketing Category Name
ANDA
Application Number
ANDA083177
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
HYDROCHLOROTHIAZIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0172-2083-80