Sodium Diuril
IntravenousSodium Diuril (chlorothiazide sodium)
Approved
Approval ID
1d9fa4e6-6516-45cd-a316-292c6a529ecc
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 1, 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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code76478-711
Application NumberNDA011145
Product Classification
M
Marketing Category
C73594
G
Generic Name
chlorothiazide sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 12, 2012
FDA Product Classification
INGREDIENTS (3)
mannitolInactive
Code: 3OWL53L36A
Classification: IACT
chlorothiazide sodiumActive
Quantity: 0.5 mg in 18 mL
Code: SN86FG7N2K
Classification: ACTIM
sodium hydroxideInactive
Code: 55X04QC32I
Classification: IACT