Package 50090-7073-1

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7073-1
Digits Only 5009070731
Product NDC 50090-7073
Product ID 50090-7073_c6ae957a-83c9-442d-89b2-9febb63c82d4
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7073-1)

Marketing

Marketing Status
Marketed Since 2024-01-23
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": "c6ae957a-83c9-442d-89b2-9febb63c82d4", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["804e873e-f48b-4c25-ad7b-41d44f61bdde"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7073-1)", "package_ndc": "50090-7073-1", "marketing_start_date": "20240123"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "50090-7073_c6ae957a-83c9-442d-89b2-9febb63c82d4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "50090-7073", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}