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HYDROCHLOROTHIAZIDE - 12634-471-91 - (HYDROCHLOROTHIAZIDE)

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Drug Information of HYDROCHLOROTHIAZIDE

Product NDC: 12634-471
Proprietary Name: HYDROCHLOROTHIAZIDE
Non Proprietary Name: HYDROCHLOROTHIAZIDE
Active Ingredient(s): 50    mg/1 & nbsp;   HYDROCHLOROTHIAZIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of HYDROCHLOROTHIAZIDE

Product NDC: 12634-471
Labeler Name: Apotheca, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084324
Marketing Category: ANDA
Start Marketing Date: 20090630

Package Information of HYDROCHLOROTHIAZIDE

Package NDC: 12634-471-91
Package Description: 1 TABLET in 1 BLISTER PACK (12634-471-91)

NDC Information of HYDROCHLOROTHIAZIDE

NDC Code 12634-471-91
Proprietary Name HYDROCHLOROTHIAZIDE
Package Description 1 TABLET in 1 BLISTER PACK (12634-471-91)
Product NDC 12634-471
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090630
Marketing Category Name ANDA
Labeler Name Apotheca, Inc.
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of HYDROCHLOROTHIAZIDE


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