# DRIZALMA SPRINKLE

NDC: 47335-616
Generic name: Duloxetine
Labeler / Manufacturer: SUN PHARMACEUTICAL INDUSTRIES, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20240610

FDA application: NDA212516

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-616"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-616
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b41423b8-dfec-4d79-ba3c-e43a87803d85