Package 72162-2418-1

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2418-1
Digits Only 7216224181
Product NDC 72162-2418
Product ID 72162-2418_098f2903-afc3-4a47-8c22-9cc1ce9d50c3
Description

100 TABLET, COATED in 1 BOTTLE (72162-2418-1)

Marketing

Marketing Status
Marketed Since 2024-10-31
Brand raloxifene hydrochloride
Generic raloxifene hydrochloride
Sample Package No

Linked Drug Pages (1)

Raloxifene hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "098f2903-afc3-4a47-8c22-9cc1ce9d50c3", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["7e4bfee5-fefc-4115-9bdb-222eccefca83"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (72162-2418-0)", "package_ndc": "72162-2418-0", "marketing_start_date": "20241031"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (72162-2418-1)", "package_ndc": "72162-2418-1", "marketing_start_date": "20241031"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72162-2418-3)", "package_ndc": "72162-2418-3", "marketing_start_date": "20241031"}], "brand_name": "Raloxifene hydrochloride", "product_id": "72162-2418_098f2903-afc3-4a47-8c22-9cc1ce9d50c3", "dosage_form": "TABLET, COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "72162-2418", "generic_name": "Raloxifene hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211324", "marketing_category": "ANDA", "marketing_start_date": "20171230", "listing_expiration_date": "20261231"}