Ciprofloxacin

Product NDC

50090-0868

11-digit product format

500900868

Labeler code

50090

Product ID

50090-0868_a538e1ac-d007-4ba5-9d91-4dc9dbe14ef3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA076558

Marketing category

ANDA

Marketing start

2004-06-09

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

2019-12-31

Current FDA listing

Historical FDA.report record