Ciprofloxacin

Product NDC

36000-011

11-digit product format

360000011

Labeler code

36000

Product ID

36000-011_8a84c55a-7ccb-4b78-988c-1a815a375370

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Baxter Healthcare Corporation

Application

ANDA078062

Marketing category

ANDA

Marketing start

2009-09-17

Marketing end

0000-00-00

Substance

CIPROFLOXACIN

Active strength

10 mg/mL

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record