# Tamsulosin hydrochloride

NDC: 76282-744
Generic name: Tamsulosin hydrochloride
Labeler / Manufacturer: EXELAN PHARMACEUTICALS, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240301

FDA application: ANDA078801

## 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:"76282-744"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-744
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db6cb771-2cff-40b7-a5ef-ea3cf2a3b461