# venlafaxine

NDC: 57237-172
Generic name: venlafaxine hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100407

FDA application: ANDA090555

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57237-172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57237-172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20319949-ccf9-477a-a6e3-53502772deb9