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Hydrochlorothiazide - 35356-702-30 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 35356-702
Proprietary Name: Hydrochlorothiazide
Non Proprietary Name: Hydrochlorothiazide
Active Ingredient(s): 25    mg/1 & nbsp;   Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrochlorothiazide

Product NDC: 35356-702
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040807
Marketing Category: ANDA
Start Marketing Date: 20110801

Package Information of Hydrochlorothiazide

Package NDC: 35356-702-30
Package Description: 30 TABLET in 1 BOTTLE (35356-702-30)

NDC Information of Hydrochlorothiazide

NDC Code 35356-702-30
Proprietary Name Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE (35356-702-30)
Product NDC 35356-702
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110801
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Hydrochlorothiazide


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