Package 0115-8211-01

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0115-8211-01
Digits Only 0115821101
Product NDC 0115-8211
Product ID 0115-8211_e62d078e-2896-4acd-bcaa-c21e855e66e1
Description

100 CAPSULE in 1 BOTTLE (0115-8211-01)

Marketing

Marketing Status
Marketed Since 2025-04-01
Brand tamsulosin hydrochloride
Generic tamsulosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Tamsulosin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e62d078e-2896-4acd-bcaa-c21e855e66e1", "openfda": {"upc": ["0301158211011"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["c3ae55dd-6a0e-4f3a-82b6-2448e0545550"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0115-8211-01)", "package_ndc": "0115-8211-01", "marketing_start_date": "20250401"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "0115-8211_e62d078e-2896-4acd-bcaa-c21e855e66e1", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0115-8211", "generic_name": "TAMSULOSIN HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA090377", "marketing_category": "ANDA", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}