Package 50090-6177-1

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6177-1
Digits Only 5009061771
Product NDC 50090-6177
Product ID 50090-6177_88a25d54-f913-4a43-9f04-9ab1979ff633
Description

90 TABLET, COATED in 1 BOTTLE (50090-6177-1)

Marketing

Marketing Status
Marketed Since 2022-10-18
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": "88a25d54-f913-4a43-9f04-9ab1979ff633", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["22a951ee-2ffc-4c60-b681-0f80285153e1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-6177-1)", "package_ndc": "50090-6177-1", "marketing_start_date": "20221018"}], "brand_name": "Raloxifene hydrochloride", "product_id": "50090-6177_88a25d54-f913-4a43-9f04-9ab1979ff633", "dosage_form": "TABLET, COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "50090-6177", "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": "ANDA211324", "marketing_category": "ANDA", "marketing_start_date": "20171230", "listing_expiration_date": "20261231"}