Package 72162-2509-1

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2509-1
Digits Only 7216225091
Product NDC 72162-2509
Description

100 CAPSULE in 1 BOTTLE (72162-2509-1)

Marketing

Marketing Status
Marketed Since 2025-05-23
Brand tamsulosin hydrochloride
Generic tamsulosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4e3d8221-3319-47d8-ba8d-1187c6dc6372", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["36b8c36f-22e5-40f5-a99a-411115f13df4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2509-1)", "package_ndc": "72162-2509-1", "marketing_start_date": "20250523"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72162-2509-5)", "package_ndc": "72162-2509-5", "marketing_start_date": "20250523"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "72162-2509_4e3d8221-3319-47d8-ba8d-1187c6dc6372", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2509", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA202433", "marketing_category": "ANDA", "marketing_start_date": "20130430", "listing_expiration_date": "20261231"}