# Venlafaxine Hydrochloride

NDC: 24658-127
Generic name: VENLAFAXINE HYDROCHLORIDE
Labeler / Manufacturer: PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260728

FDA application: ANDA214654

## 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:"24658-127"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24658-127
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b1d21366-f686-4e20-a10f-0c25f517db38