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FDA Product

Sodium Diuril

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Sodium Diuril

76478-711

Regulatory Information

76478-711

NDA011145

C73594

June 12, 2012

USA

IntravenousSodium Diuril (chlorothiazide sodium)

HUMAN PRESCRIPTION DRUG LABEL

11

Company Information

Akorn

117693100

Active Ingredients

mannitol

Code: 3OWL53L36A

Class Code: IACT

chlorothiazide sodium

Quantity: 0.5 mg in 18 mL

Code: SN86FG7N2K

Class Code: ACTIM

sodium hydroxide

Code: 55X04QC32I

Class Code: IACT

Active Moieties

chlorothiazide

Code: 77W477J15H

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