Chloroquine Phosphate
Chloroquine Phosphate Tablets, USP
Approved
Approval ID
cc0cb812-48f9-a138-e053-2a95a90a7666
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 9, 2024
Manufacturers
FDA
Suven Pharmaceuticals Limited
DUNS: 677604288
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Chloroquine Phosphate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68022-0265
Application NumberANDA214756
Product Classification
M
Marketing Category
C73584
G
Generic Name
Chloroquine Phosphate
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 9, 2024
FDA Product Classification
INGREDIENTS (1)
CHLOROQUINE PHOSPHATEActive
Quantity: 500 mg in 1 1
Code: 6E17K3343P
Classification: ACTIB
Chloroquine Phosphate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68022-0264
Application NumberANDA214756
Product Classification
M
Marketing Category
C73584
G
Generic Name
Chloroquine Phosphate
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 9, 2024
FDA Product Classification
INGREDIENTS (1)
CHLOROQUINE PHOSPHATEActive
Quantity: 500 mg in 1 1
Code: 6E17K3343P
Classification: ACTIB