Package 68462-393-23

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68462-393-23
Digits Only 6846239323
Product NDC 68462-393
Product ID 68462-393_3681932a-8ad0-4486-ae11-efc2f4b3ee96
Description

2000 TABLET, FILM COATED in 1 BOTTLE (68462-393-23)

Marketing

Marketing Status
Marketed Since 2016-03-22
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": "3681932a-8ad0-4486-ae11-efc2f4b3ee96", "openfda": {"upc": ["0368462393017"], "unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["c05521f8-95d2-44b8-8433-eba539c0f84c"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-393-01)", "package_ndc": "68462-393-01", "marketing_start_date": "20160322"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68462-393-10)", "package_ndc": "68462-393-10", "marketing_start_date": "20160322"}, {"sample": false, "description": "2000 TABLET, FILM COATED in 1 BOTTLE (68462-393-23)", "package_ndc": "68462-393-23", "marketing_start_date": "20160322"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68462-393-30)", "package_ndc": "68462-393-30", "marketing_start_date": "20160322"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68462-393-90)", "package_ndc": "68462-393-90", "marketing_start_date": "20160322"}], "brand_name": "raloxifene hydrochloride", "product_id": "68462-393_3681932a-8ad0-4486-ae11-efc2f4b3ee96", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "68462-393", "generic_name": "raloxifene hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "raloxifene hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204491", "marketing_category": "ANDA", "marketing_start_date": "20160322", "listing_expiration_date": "20261231"}