NDC 0093-1010 – Mupirocin

Mupirocin 20 mg/g · Ointment · Topical

Human Prescription Drug 1 recall

Product NDC0093-1010

Product details

Brand name
Mupirocin
Generic name
Mupirocin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Ointment
Route
Topical
Marketing category
ANDA · ANDA065085
Marketed since
November 7, 2003
Listing expires
December 31, 2026
Pharmacologic class
RNA Synthetase Inhibitor Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Mupirocin →

Package NDC codes (1)

Package NDCDescriptionSince
0093-1010-421 TUBE in 1 CARTON (0093-1010-42) / 22 g in 1 TUBENov 7, 2003

Recalls mentioning this NDC

Other Mupirocin products