Ciprofloxacin

Product NDC

71335-1190

11-digit product format

713351190

Labeler code

71335

Product ID

71335-1190_1337559f-382e-4bfd-887b-50280510b53e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076126

Marketing category

ANDA

Marketing start

2009-10-10

Marketing end

0000-00-00

Substance

CIPROFLOXACIN HYDROCHLORIDE

Active strength

250 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