NDC 55150-234 – Polymyxin B

Polymyxin B Sulfate 500000 [USP'U]/1 · Injection, Powder, Lyophilized, For Solution · Intramuscular, Intrathecal, Intravenous, Ophthalmic

Human Prescription Drug 1 recall

Product NDC55150-234

Product details

Brand name
Polymyxin B
Generic name
Polymyxin B
Labeler
Eugia US LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intramuscular, Intrathecal, Intravenous, Ophthalmic
Marketing category
ANDA · ANDA206589
Marketed since
April 4, 2016
Listing expires
December 31, 2026
Pharmacologic class
Polymyxin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Polymyxin B →

Package NDC codes (1)

Package NDCDescriptionSince
55150-234-1010 VIAL in 1 CARTON (55150-234-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIALApr 4, 2016

Recalls mentioning this NDC

Other Polymyxin B products