Avelox

Product NDC

50419-530

11-digit product format

504190530

Labeler code

50419

Product ID

50419-530_308257f1-8828-4071-b009-402d9092bd2d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

moxifloxacin hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bayer HealthCare Pharmaceuticals Inc.

Application

NDA021085

Marketing category

NDA

Marketing start

1999-12-10

Marketing end

2019-06-30

Substance

MOXIFLOXACIN HYDROCHLORIDE

Active strength

400 mg/1

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record