# Tobramycin

NDC: 63323-306
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: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20051123

FDA application: ANDA065122

## 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:"63323-306"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-306
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0b4a4b00-7f78-4e95-b870-f88fea73348e