# Venlafaxine Hydrochloride

NDC: 70518-2259
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190809

FDA application: ANDA200834

## 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:"70518-2259"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2259
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=50d3b487-9f65-4e2f-b6eb-9533964f8972