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Tobramycin

NDC 39822-0412 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerXGen Pharmaceuticals DJB, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065013
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsTOBRAMYCIN SULFATE (1.2 g/30mL)
Marketing started20010817
Package count2

External sources

Source: openFDA. Public-domain (CC0).