Ciprofloxacin

Product NDC

68788-9330

11-digit product format

687889330

Labeler code

68788

Product ID

68788-9330_55dad190-5976-438d-96c8-225c5b11cdd7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA076794

Marketing category

ANDA

Marketing start

2014-10-21

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

2019-12-31

Current FDA listing

Historical FDA.report record