# Venlafaxine Hydrochloride

NDC: 70010-186
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230925

FDA application: ANDA217390

## 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:"70010-186"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-186
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=67059969-e291-4609-b130-0faacf2a19f0