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Hydrochlorothiazide - 52125-216-02 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 52125-216
Proprietary Name: Hydrochlorothiazide
Non Proprietary Name: Hydrochlorothiazide
Active Ingredient(s): 12.5    mg/1 & nbsp;   Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrochlorothiazide

Product NDC: 52125-216
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020504
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130327

Package Information of Hydrochlorothiazide

Package NDC: 52125-216-02
Package Description: 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (52125-216-02)

NDC Information of Hydrochlorothiazide

NDC Code 52125-216-02
Proprietary Name Hydrochlorothiazide
Package Description 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (52125-216-02)
Product NDC 52125-216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20130327
Marketing Category Name NDA AUTHORIZED GENERIC
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


General Information