# VENLAFAXINE HYDROCHLORIDE

NDC: 72603-749
Generic name: VENLAFAXINE HYDROCHLORIDE
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260601

FDA application: ANDA217767

## 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:"72603-749"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-749
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b865c175-e75d-4cb4-ac29-dec72226302c