# Tamsulosin Hydrochloride

NDC: 65862-598
Generic name: Tamsulosin Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20130430

FDA application: ANDA202433

## 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:"65862-598"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-598
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8cb27f78-2d5d-4640-b7b5-ed06973c8133