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COLISTIMETHATE SODIUM

NDC 23155-193 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202359
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCOLISTIMETHATE SODIUM (150 mg/4mL)
Marketing started20210909
Package count2

External sources

Source: openFDA. Public-domain (CC0).