# Desvenlafaxine

NDC: 46708-152
Generic name: Desvenlafaxine
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20130305

FDA application: NDA204150

## Active ingredients

- DESVENLAFAXINE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-152"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-152
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f74708c-6f6a-46cf-8c79-87a25c2bb6f8
