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Chlorthalidone - 21695-671-30 - (chlorthalidone)

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Drug Information of Chlorthalidone

Product NDC: 21695-671
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: 21695-671
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086831
Marketing Category: ANDA
Start Marketing Date: 20091118

Package Information of Chlorthalidone

Package NDC: 21695-671-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (21695-671-30)

NDC Information of Chlorthalidone

NDC Code 21695-671-30
Proprietary Name Chlorthalidone
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (21695-671-30)
Product NDC 21695-671
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091118
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CHLORTHALIDONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of Chlorthalidone


General Information