# venlafaxine hydrochloride, extended release

NDC: 42799-962
Generic name: venlafaxine hydrochloride, extended release
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230315

FDA application: ANDA209193

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42799-962"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-962
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=38431a76-6185-4c17-994f-8278b6cd7510