|
CiprofloxacinDrug - Ciprofloxacin The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Ciprofloxacin Hydrochloride
Strength -
EQ 750MG BASE
Applicant -
UNIQUE PHARM LABS
New Drug Application (NDA) Number -
076639
Product Number -
003
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Sep 10, 2004
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Unique Pharmaceutical Laboratories
Ciprofloxacin
Ciprofloxacin Eq 500mg Base Tablet; Oral
Ciprofloxacin Eq 750mg Base Tablet; Oral Ciprofloxacin Eq 750mg Base Tablet; Oral Ciprofloxacin Eq 250mg Base Tablet; Oral Ciprofloxacin Eq 500mg Base Tablet; Oral Ciprofloxacin Eq 750mg Base Tablet; Oral Ciprofloxacin Eq 250mg Base Tablet; Oral Ciprofloxacin Eq 500mg Base Tablet; Oral Ciprofloxacin Eq 750mg Base Tablet; Oral Ciprofloxacin Eq 250mg Base Tablet; Oral NewDrugInformation |