Clindamycin Phosphate
Clindamycin Phosphate Gel USP, 1% For External Use
Approved
Approval ID
b46941a9-e75f-48f7-b426-03f307499713
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 11, 2023
Manufacturers
FDA
Solaris Pharma Corporation
DUNS: 079904672
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
clindamycin phosphate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code73473-300
Application NumberANDA211872
Product Classification
M
Marketing Category
C73584
G
Generic Name
clindamycin phosphate
Product Specifications
Route of AdministrationTOPICAL
Effective DateAugust 11, 2023
FDA Product Classification
INGREDIENTS (1)
CLINDAMYCIN PHOSPHATEActive
Quantity: 10 mg in 1 g
Code: EH6D7113I8
Classification: ACTIM