Package 50268-694-15
Brand: raloxifene hydrochloride
Generic: raloxifene hydrochloridePackage Facts
Identity
Package NDC
50268-694-15
Digits Only
5026869415
Product NDC
50268-694
Description
50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-694-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-694-11)
Marketing
Marketing Status
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": "48255cf3-7607-03f0-e063-6394a90ae486", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["6f7eb934-aa60-51e1-e053-2a91aa0a3914"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-694-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-694-11)", "package_ndc": "50268-694-15", "marketing_start_date": "20180627"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "50268-694_48255cf3-7607-03f0-e063-6394a90ae486", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "50268-694", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208206", "marketing_category": "ANDA", "marketing_start_date": "20180627", "listing_expiration_date": "20271231"}