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Captopril and Hydrochlorothiazide - 54868-5787-0 - (Captopril and Hydrochlorothiazide)

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Drug Information of Captopril and Hydrochlorothiazide

Product NDC: 54868-5787
Proprietary Name: Captopril and Hydrochlorothiazide
Non Proprietary Name: Captopril and Hydrochlorothiazide
Active Ingredient(s): 25; 25    mg/1; mg/1 & nbsp;   Captopril and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Captopril and Hydrochlorothiazide

Product NDC: 54868-5787
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074896
Marketing Category: ANDA
Start Marketing Date: 20070712

Package Information of Captopril and Hydrochlorothiazide

Package NDC: 54868-5787-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-5787-0)

NDC Information of Captopril and Hydrochlorothiazide

NDC Code 54868-5787-0
Proprietary Name Captopril and Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-5787-0)
Product NDC 54868-5787
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Captopril and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070712
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CAPTOPRIL; HYDROCHLOROTHIAZIDE
Strength Number 25; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Captopril and Hydrochlorothiazide


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