Ciprofloxacin

Product NDC

70518-1975

11-digit product format

705181975

Labeler code

70518

Product ID

70518-1975_84b4c3d2-9c55-ca6e-e053-2a91aa0a0103

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076126

Marketing category

ANDA

Marketing start

2019-03-22

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