VIGAMOX

Product NDC

70518-2043

11-digit product format

705182043

Labeler code

70518

Product ID

70518-2043_970fa816-6e28-b4e6-e053-2995a90a78d0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

moxifloxacin hydrochloride

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

REMEDYREPACK INC.

Application

NDA021598

Marketing category

NDA

Marketing start

2019-04-26

Marketing end

0000-00-00

Substance

MOXIFLOXACIN HYDROCHLORIDE

Active strength

5 mg/mL

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record