# Tafluprost

NDC: 0781-6184
Generic name: Tafluprost
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20221205

FDA application: ANDA209040

## Active ingredients

- TAFLUPROST: .0045 mg/.3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-6184"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-6184
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bfffa484-4105-45ec-ab1d-124e96639f35