# Venlafaxine Hydrochloride

NDC: 60760-836
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: ST. MARY'S MEDICAL PARK PHARMACY
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20110601

FDA application: ANDA200834

## 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:"60760-836"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-836
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=35d3148b-52f3-197c-e063-6294a90a44e3