# Tobramycin

NDC: 63323-303
Generic name: TOBRAMYCIN SULFATE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20051123

FDA application: NDA050789

## Active ingredients

- TOBRAMYCIN SULFATE: 1200 mg/30mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-303"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-303
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9a5cecd6-aa65-42d2-b15a-06b4fcebcc0f