Package 71335-2059-1

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2059-1
Digits Only 7133520591
Product NDC 71335-2059
Description

60 TABLET, FILM COATED in 1 BOTTLE (71335-2059-1)

Marketing

Marketing Status
Marketed Since 2022-03-03
Brand raloxifene hydrochloride
Generic raloxifene hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7a2ab3a6-eba9-4ac6-ba53-3940b614102d", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["5a22ae27-1c55-487b-8e93-8ef1cec87065"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2059-1)", "package_ndc": "71335-2059-1", "marketing_start_date": "20220303"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2059-2)", "package_ndc": "71335-2059-2", "marketing_start_date": "20240227"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "71335-2059_7a2ab3a6-eba9-4ac6-ba53-3940b614102d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "71335-2059", "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": "ANDA204310", "marketing_category": "ANDA", "marketing_start_date": "20150828", "listing_expiration_date": "20261231"}