Skip to main content

Polymyxin B

NDC 0143-9941 · Hikma Pharmaceuticals USA Inc.

Generic namePolymyxin B sulfate
Dosage formINJECTION, POWDER, FOR SOLUTION
RouteINTRAMUSCULAR, INTRATHECAL, INTRAVENOUS, OPHTHALMIC
Active ingredient(s)POLYMYXIN B SULFATE
Strength500000 [iU]/1
Pharmacologic classPolymyxin-class Antibacterial [EPC], Polymyxins [CS]
Marketing categoryANDA

Packages

0143-9941-10 — 10 VIAL in 1 CARTON (0143-9941-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9941-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0078-0771 — neomycin sulfate, polymyxin b sulfate and dexamethasone, 0113-0084 — bacitracin zinc, neomycin, polymyxin B, 0113-0679 — Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl, 0113-1140 — Bacitracin Zinc, Neomycin sulfate, Polymyxin B, Pramoxine HCl, 0143-9461 — Polymyxin B Sulfate, 0363-0018 — Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, 0363-0539 — bacitracin zinc, neomycin, polymyxin B, 0363-0841 — Bacitracin Zinc, Neomycin sulfate, Polymyxin B, Pramoxine HCl, 0363-1331 — Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, 0363-1332 — bacitracin zinc, neomycin sulfate, polymyxin b sulfate, 0363-2122 — Polymyxin B Sulfate, Neomycin Sulfate, Pramoxine Hydrochloride, 0363-2123 — Polymyxin B Sulfate, Neomycin Sulfate, Pramoxine Hydrochloride, 0363-6790 — Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl, 0363-8888 — bacitracin zinc, neomycin sulfate, polymyxin B sulfate, and pramoxine hydrochloride, 0404-0167 — Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate, 0404-0171 — Bacitracin Zinc, Polymyxin B Sulfate, and Neomycin Sulfate, 0713-0268 — Polymyxin B Sulfate, Bacitracin Zinc and Neomycin Sulfate, 0713-0622 — Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate, Pramoxine HCl, 0904-8805 — Bacitracin Zinc, Neomycin, Polymyxin B Sulfat, 0924-5604 — bacitracin zinc, neomycin sulfate, polymyxin b sulfate, +354 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.