Ciprofloxacin

Product NDC

55700-744

11-digit product format

557000744

Labeler code

55700

Product ID

55700-744_85182e1b-f475-4390-9caa-9343b6260c23

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Quality Care Products, LLC

Application

ANDA076126

Marketing category

ANDA

Marketing start

2019-04-11

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