Ciprofloxacin

Product NDC

63187-250

11-digit product format

631870250

Labeler code

63187

Product ID

63187-250_e44561c3-294b-46e5-82ce-20af0c6e6f0a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA076558

Marketing category

ANDA

Marketing start

2004-06-09

Marketing end

0000-00-00

Substance

CIPROFLOXACIN HYDROCHLORIDE

Active strength

500 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