# Tobramycin

NDC: 63323-307
Generic name: TOBRAMYCIN SULFATE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20041130

FDA application: ANDA065120

## Active ingredients

- TOBRAMYCIN SULFATE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-307"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-307
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8cfeb84f-193a-458a-bdec-205d9274e1a4