Package 71335-1715-1

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1715-1
Digits Only 7133517151
Product NDC 71335-1715
Product ID 71335-1715_8f53d830-2fb0-400c-8f03-f81858280782
Description

60 TABLET, FILM COATED in 1 BOTTLE (71335-1715-1)

Marketing

Marketing Status
Marketed Since 2020-10-02
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": "8f53d830-2fb0-400c-8f03-f81858280782", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["3568ed3c-6afd-4872-a861-93a7873bec9c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1715-1)", "package_ndc": "71335-1715-1", "marketing_start_date": "20201002"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1715-2)", "package_ndc": "71335-1715-2", "marketing_start_date": "20211229"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "71335-1715_8f53d830-2fb0-400c-8f03-f81858280782", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "71335-1715", "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": "ANDA078193", "marketing_category": "ANDA", "marketing_start_date": "20140328", "listing_expiration_date": "20261231"}