Avelox

Product NDC

50419-537

11-digit product format

504190537

Labeler code

50419

Product ID

50419-537_9cae0b2d-5feb-4962-9ee2-2a49642f26c3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

moxifloxacin hydrochloride

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Bayer HealthCare Pharmaceuticals Inc.

Application

NDA021277

Marketing category

NDA

Marketing start

2001-11-30

Marketing end

2020-06-01

Substance

MOXIFLOXACIN HYDROCHLORIDE

Active strength

400 mg/250mL

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record