# Venlafaxine

NDC: 67877-726
Generic name: Venlafaxine
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210611

FDA application: ANDA214127

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-726"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-726
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=528d5392-4ad5-48c5-963d-6ebfb9187db4