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Hydrochlorothiazide - 65862-113-01 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 65862-113
Proprietary Name: Hydrochlorothiazide
Non Proprietary Name: Hydrochlorothiazide
Active Ingredient(s): 12.5    mg/1 & nbsp;   Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrochlorothiazide

Product NDC: 65862-113
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078164
Marketing Category: ANDA
Start Marketing Date: 20070919

Package Information of Hydrochlorothiazide

Package NDC: 65862-113-01
Package Description: 100 CAPSULE in 1 BOTTLE (65862-113-01)

NDC Information of Hydrochlorothiazide

NDC Code 65862-113-01
Proprietary Name Hydrochlorothiazide
Package Description 100 CAPSULE in 1 BOTTLE (65862-113-01)
Product NDC 65862-113
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070919
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Hydrochlorothiazide


General Information