# Desvenlafaxine

NDC: 60687-607
Generic name: Desvenlafaxine
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20211201

FDA application: ANDA204082

## Active ingredients

- DESVENLAFAXINE SUCCINATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-607"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-607
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e0dbbdbc-9438-407a-b3e1-f3bb7f177a4e