Ciprofloxacin

Product NDC

51079-182

11-digit product format

510790182

Labeler code

51079

Product ID

51079-182_7baba049-e06c-70a7-e053-2991aa0a08a8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ciprofloxacin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA075817

Marketing category

ANDA

Marketing start

2011-04-11

Marketing end

2020-03-31

Substance

CIPROFLOXACIN HYDROCHLORIDE

Active strength

500 mg/1

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record