# tamsulosin hydrochloride

NDC: 72865-350
Generic name: tamsulosin hydrochloride
Labeler / Manufacturer: XLCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260101

FDA application: ANDA214730

## Active ingredients

- TAMSULOSIN HYDROCHLORIDE: .4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72865-350"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72865-350
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=00097e78-9c04-4e62-8260-ddb50e9a6a93