Cipro

Product NDC

50419-789

11-digit product format

504190789

Labeler code

50419

Product ID

50419-789_6a45ebbd-49c4-4177-8ee3-ad4e02b780da

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ciprofloxacin

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Bayer HealthCare Pharmaceuticals Inc.

Application

NDA021473

Marketing category

NDA

Marketing start

2012-10-01

Marketing end

0000-00-00

Substance

CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE

Active strength

452 mg/1; 1/1

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS],Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record