# venlafaxine

NDC: 52427-632
Generic name: venlafaxine
Labeler / Manufacturer: Almatica Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220630

FDA application: NDA215429

## Active ingredients

- VENLAFAXINE BESYLATE MONOHYDRATE: 112.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52427-632"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52427-632
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e81a2daf-b8b2-7c05-b532-bc775700b100