Moxifloxacin Hydrochloride

Product NDC

47781-268

11-digit product format

477810268

Labeler code

47781

Product ID

47781-268_7224ee30-a17d-41c3-867c-b4466be8e434

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

moxifloxacin hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Alvogen, Inc.

Application

NDA021085

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-01-29

Marketing end

0000-00-00

Substance

MOXIFLOXACIN HYDROCHLORIDE

Active strength

400 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