Package 71610-524-60

Brand: raloxifene hydrochloride

Generic: raloxifene
NDC Package

Package Facts

Identity

Package NDC 71610-524-60
Digits Only 7161052460
Product NDC 71610-524
Product ID 71610-524_4dfb7a20-54ea-4e48-9f0d-03099593073f
Description

90 TABLET in 1 BOTTLE (71610-524-60)

Marketing

Marketing Status
Marketed Since 2021-02-03
Brand raloxifene hydrochloride
Generic raloxifene
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": "4dfb7a20-54ea-4e48-9f0d-03099593073f", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["53a2db10-4af8-4032-b598-b7c7a0969801"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-524-60)", "package_ndc": "71610-524-60", "marketing_start_date": "20210203"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "71610-524_4dfb7a20-54ea-4e48-9f0d-03099593073f", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "71610-524", "generic_name": "Raloxifene", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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": "20160629", "listing_expiration_date": "20261231"}