Cipro

Product NDC

50419-759

11-digit product format

504190759

Labeler code

50419

Product ID

50419-759_f94f3800-252e-4b03-823a-099d24abc301

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ciprofloxacin

Dosage form

SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Bayer HealthCare Pharmaceuticals Inc.

Application

NDA019857

Marketing category

NDA

Marketing start

2009-04-22

Marketing end

0000-00-00

Substance

CIPROFLOXACIN

Active strength

2 mg/mL

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record