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Hydrochlorothiazide - 0527-1635-10 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 0527-1635
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: 0527-1635
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091662
Marketing Category: ANDA
Start Marketing Date: 20120127

Package Information of Hydrochlorothiazide

Package NDC: 0527-1635-10
Package Description: 1000 CAPSULE in 1 BOTTLE (0527-1635-10)

NDC Information of Hydrochlorothiazide

NDC Code 0527-1635-10
Proprietary Name Hydrochlorothiazide
Package Description 1000 CAPSULE in 1 BOTTLE (0527-1635-10)
Product NDC 0527-1635
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120127
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
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