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Hydrochlorothiazide - 49349-721-02 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 49349-721
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: 49349-721
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040807
Marketing Category: ANDA
Start Marketing Date: 20110830

Package Information of Hydrochlorothiazide

Package NDC: 49349-721-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-721-02)

NDC Information of Hydrochlorothiazide

NDC Code 49349-721-02
Proprietary Name Hydrochlorothiazide
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-721-02)
Product NDC 49349-721
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110830
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


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