Package 50228-306-30

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50228-306-30
Digits Only 5022830630
Product NDC 50228-306
Product ID 50228-306_f1da5bd3-72c2-15ff-e053-2995a90a89db
Description

30 TABLET, FILM COATED in 1 BOTTLE (50228-306-30)

Marketing

Marketing Status
Marketed Since 2016-10-12
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": "f1da5bd3-72c2-15ff-e053-2995a90a89db", "openfda": {"upc": ["0350228306201", "0350228306300"], "unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["8152e68b-61a8-4897-8e03-900135b1dbd5"], "manufacturer_name": ["ScieGen Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2000 TABLET, FILM COATED in 1 BOTTLE (50228-306-20)", "package_ndc": "50228-306-20", "marketing_start_date": "20161012"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-306-30)", "package_ndc": "50228-306-30", "marketing_start_date": "20161012"}], "brand_name": "Raloxifene hydrochloride", "product_id": "50228-306_f1da5bd3-72c2-15ff-e053-2995a90a89db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "50228-306", "generic_name": "Raloxifene hydrochloride", "labeler_name": "ScieGen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA206384", "marketing_category": "ANDA", "marketing_start_date": "20161012", "listing_expiration_date": "20261231"}