Package 76282-256-30

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76282-256-30
Digits Only 7628225630
Product NDC 76282-256
Product ID 76282-256_7238f870-72f1-4e67-9c88-5125522971da
Description

30 TABLET, FILM COATED in 1 BOTTLE (76282-256-30)

Marketing

Marketing Status
Marketed Since 2014-11-12
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": "7238f870-72f1-4e67-9c88-5125522971da", "openfda": {"upc": ["0376282256306"], "unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["2b94ecf5-d870-4132-b455-d5ee5c9dce56"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76282-256-01)", "package_ndc": "76282-256-01", "marketing_start_date": "20141112"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76282-256-05)", "package_ndc": "76282-256-05", "marketing_start_date": "20141112"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (76282-256-10)", "package_ndc": "76282-256-10", "marketing_start_date": "20150415"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76282-256-30)", "package_ndc": "76282-256-30", "marketing_start_date": "20141112"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76282-256-90)", "package_ndc": "76282-256-90", "marketing_start_date": "20150415"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "76282-256_7238f870-72f1-4e67-9c88-5125522971da", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "76282-256", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "Exelan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090842", "marketing_category": "ANDA", "marketing_start_date": "20141112", "listing_expiration_date": "20261231"}