# duloxetine

NDC: 70247-014
Generic name: Duloxetine
Labeler / Manufacturer: Qingdao BAHEAL Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20180505

FDA application: ANDA210599

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70247-014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70247-014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e428429e-e1ea-40e1-870f-134533dc3aa1