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Chlorothiazide - 63323-658-27 - (CHLOROTHIAZIDE SODIUM)

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Drug Information of Chlorothiazide

Product NDC: 63323-658
Proprietary Name: Chlorothiazide
Non Proprietary Name: CHLOROTHIAZIDE SODIUM
Active Ingredient(s): 500    mg/18mL & nbsp;   CHLOROTHIAZIDE SODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Chlorothiazide

Product NDC: 63323-658
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090896
Marketing Category: ANDA
Start Marketing Date: 20091021

Package Information of Chlorothiazide

Package NDC: 63323-658-27
Package Description: 1 VIAL in 1 BOX (63323-658-27) > 18 mL in 1 VIAL

NDC Information of Chlorothiazide

NDC Code 63323-658-27
Proprietary Name Chlorothiazide
Package Description 1 VIAL in 1 BOX (63323-658-27) > 18 mL in 1 VIAL
Product NDC 63323-658
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CHLOROTHIAZIDE SODIUM
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091021
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name CHLOROTHIAZIDE SODIUM
Strength Number 500
Strength Unit mg/18mL
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Chlorothiazide


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