Ciprofloxacin
CIPROFLOXACIN 500 mg
Approved
Approval ID
6f41228b-974a-443b-a313-2fbb3d845915
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 16, 2010
Manufacturers
FDA
Testpak Holding Company
DUNS: 108660077
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ciprofloxacin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code53401-004
Application NumberANDA007581
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ciprofloxacin
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 16, 2010
FDA Product Classification
INGREDIENTS (1)
CiprofloxacinActive
Quantity: 500 mg in 1 1
Code: 5E8K9I0O4U
Classification: ACTIB