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Polymyxin B

NDC 0143-9461 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic namePolymyxin B Sulfate
Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202766
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRATHECAL INTRAVENOUS OPHTHALMIC
Active ingredientsPOLYMYXIN B SULFATE (500000 [USP'U]/1)
Marketing started20250930
Package count2

External sources

Source: openFDA. Public-domain (CC0).