Ciprofloxacin

Product NDC

0179-0188

11-digit product format

001790188

Labeler code

0179

Product ID

0179-0188_7b96c5d0-d0a7-444e-e053-2a91aa0a3e89

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

ANDA076558

Marketing category

ANDA

Marketing start

2015-10-29

Marketing end

2020-08-31

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