Ciprofloxacin

Product NDC

59115-029

11-digit product format

591150029

Labeler code

59115

Product ID

59115-029_5268c4b9-0e68-4aa2-a75b-5ed1e77c4318

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Hikma Pharmaceutical

Application

ANDA076558

Marketing category

ANDA

Marketing start

2004-06-09

Marketing end

0000-00-00

Substance

CIPROFLOXACIN HYDROCHLORIDE

Active strength

500 mg/1

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record