Moxifloxacin

Product NDC

55700-638

11-digit product format

557000638

Labeler code

55700

Product ID

55700-638_e4660daa-ec06-4c67-881f-8b761f20d9ea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Moxifloxacin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076938

Marketing category

ANDA

Marketing start

2018-06-15

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

2019-12-31

Current FDA listing

Historical FDA.report record