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Hydrochlorothiazide - 49349-780-02 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 49349-780
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: 49349-780
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040412
Marketing Category: ANDA
Start Marketing Date: 20110927

Package Information of Hydrochlorothiazide

Package NDC: 49349-780-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-780-02)

NDC Information of Hydrochlorothiazide

NDC Code 49349-780-02
Proprietary Name Hydrochlorothiazide
Package Description 30 TABLET in 1 BLISTER PACK (49349-780-02)
Product NDC 49349-780
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110927
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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