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Chlorthalidone - 54868-2007-1 - (Chlorthalidone)

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Drug Information of Chlorthalidone

Product NDC: 54868-2007
Proprietary Name: Chlorthalidone
Non Proprietary Name: Chlorthalidone
Active Ingredient(s): 25    mg/1 & nbsp;   Chlorthalidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Chlorthalidone

Product NDC: 54868-2007
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086831
Marketing Category: ANDA
Start Marketing Date: 20030609

Package Information of Chlorthalidone

Package NDC: 54868-2007-1
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (54868-2007-1)

NDC Information of Chlorthalidone

NDC Code 54868-2007-1
Proprietary Name Chlorthalidone
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (54868-2007-1)
Product NDC 54868-2007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030609
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CHLORTHALIDONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of Chlorthalidone


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