# TAMSULOSIN HYDROCHLORIDE

NDC: 61919-703
Generic name: TAMSULOSIN HYDROCHLORIDE
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190717

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:"61919-703"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-703
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8de50eca-8cc5-082d-e053-2a95a90a346d