Package 72162-2217-5

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2217-5
Digits Only 7216222175
Product NDC 72162-2217
Product ID 72162-2217_566e638b-1851-45e0-b04e-9c547be44c27
Description

500 CAPSULE in 1 BOTTLE (72162-2217-5)

Marketing

Marketing Status
Marketed Since 2024-01-05
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": "566e638b-1851-45e0-b04e-9c547be44c27", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["fd73ddfd-3773-45b2-9795-9e58744a6803"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72162-2217-5)", "package_ndc": "72162-2217-5", "marketing_start_date": "20240105"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "72162-2217_566e638b-1851-45e0-b04e-9c547be44c27", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2217", "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"}