Chlorothiazide Sodium
Chlorothiazide Sodium for Injection, USP
Approved
Approval ID
5046a4d7-7742-4f19-930a-2582cb41474e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 29, 2022
Manufacturers
FDA
Akorn
DUNS: 117693100
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Chlorothiazide Sodium
PRODUCT DETAILS
NDC Product Code17478-419
Application NumberNDA011145
Marketing CategoryC73605
Route of AdministrationINTRAVENOUS
Effective DateAugust 10, 2012
Generic NameChlorothiazide Sodium
INGREDIENTS (3)
Sodium HydroxideInactive
Code: 55X04QC32I
Classification: IACT
MannitolInactive
Quantity: 250 mg in 1 1
Code: 3OWL53L36A
Classification: IACT
Chlorothiazide SodiumActive
Quantity: 500 mg in 1 1
Code: SN86FG7N2K
Classification: ACTIM