Moxifloxacin Hydrochloride

Product NDC

43063-580

11-digit product format

430630580

Labeler code

43063

Product ID

43063-580_96235914-eb46-1e33-e053-2995a90a2695

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

moxifloxacin hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, 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