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hydrochlorothiazide - 35356-807-60 - (hydrochlorothiazide)

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Drug Information of hydrochlorothiazide

Product NDC: 35356-807
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: 35356-807
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090510
Marketing Category: ANDA
Start Marketing Date: 20100315

Package Information of hydrochlorothiazide

Package NDC: 35356-807-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (35356-807-60)

NDC Information of hydrochlorothiazide

NDC Code 35356-807-60
Proprietary Name hydrochlorothiazide
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (35356-807-60)
Product NDC 35356-807
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100315
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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


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