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Hydrochlorothiazide - 43063-412-30 - (Hydrochlorothiazide)

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Drug Information of Hydrochlorothiazide

Product NDC: 43063-412
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: 43063-412
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091662
Marketing Category: ANDA
Start Marketing Date: 20120127

Package Information of Hydrochlorothiazide

Package NDC: 43063-412-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-412-30)

NDC Information of Hydrochlorothiazide

NDC Code 43063-412-30
Proprietary Name Hydrochlorothiazide
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-412-30)
Product NDC 43063-412
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120127
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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