mupirocin

Product NDC

50268-572

11-digit product format

502680572

Labeler code

50268

Product ID

50268-572_9c96ef33-8039-49fd-e053-2a95a90a24ec

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mupirocin

Dosage form

OINTMENT

Route

TOPICAL

Labeler

AvPAK

Application

ANDA065123

Marketing category

ANDA

Marketing start

2016-09-14

Marketing end

0000-00-00

Substance

MUPIROCIN

Active strength

20 mg/g

Pharmacologic classes

RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record