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"59762-1736-7" National Drug Code (NDC)
Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (59762-1736-7)
(Greenstone LLC)
NDC Code
59762-1736-7
Package Description
1000 TABLET in 1 BOTTLE (59762-1736-7)
Product NDC
59762-1736
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydrochlorothiazide
Non-Proprietary Name
Hydrochlorothiazide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070720
End Marketing Date
20140630
Marketing Category Name
ANDA
Application Number
ANDA040780
Manufacturer
Greenstone LLC
Substance Name
HYDROCHLOROTHIAZIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-1736-7