# Oseltamivir Phosphate

NDC: 0093-8180
Generic name: Oseltamivir Phosphate
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20190710

FDA application: ANDA211125

## Active ingredients

- OSELTAMIVIR PHOSPHATE: 6 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-8180"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-8180
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ea5bf8f-c3fa-4d44-bc3d-b1912374ee4b