Ciprofloxacin

Product NDC

24658-185

11-digit product format

246580185

Labeler code

24658

Product ID

24658-185_39508205-af8a-4ace-9353-84c39d98fdeb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin

Dosage form

TABLET

Route

ORAL

Labeler

PuraCap Laboratories LLC dba Blu Pharmaceuticals

Application

ANDA076639

Marketing category

ANDA

Marketing start

2004-09-10

Marketing end

2020-05-31

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