# VENLAFAXINE

NDC: 71209-026
Generic name: venlafaxine
Labeler / Manufacturer: Cadila Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181203

FDA application: ANDA206250

## 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:"71209-026"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71209-026
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2ed61dcf-42e3-47cf-a607-459eef5fea98