Ciprofloxacin

Product NDC

68071-4403

11-digit product format

680714403

Labeler code

68071

Product ID

68071-4403_6aae10db-25d8-cb66-e053-2991aa0a2a30

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin Hydrochloride

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA076555

Marketing category

ANDA

Marketing start

2009-07-24

Marketing end

0000-00-00

Substance

CIPROFLOXACIN HYDROCHLORIDE

Active strength

3 mg/mL

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record