ciprofloxacin hydrochloride
CIPROFLOXACIN TABLETS, USP
Approved
Approval ID
8c353bf4-f26b-4ab8-9694-aa9f10dfe965
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 12, 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 hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code53401-005
Application NumberANDA076794
Product Classification
M
Marketing Category
C73584
G
Generic Name
ciprofloxacin hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 12, 2010
FDA Product Classification
INGREDIENTS (1)
ciprofloxacin hydrochlorideActive
Quantity: 500 mg in 1 1
Code: 4BA73M5E37
Classification: ACTIB