Package 0904-6902-04

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6902-04
Digits Only 0904690204
Product NDC 0904-6902
Product ID 0904-6902_ae852e8a-bdc7-4062-8939-d5c58768e2bb
Description

30 BLISTER PACK in 1 CARTON (0904-6902-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2016-10-12
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": "ae852e8a-bdc7-4062-8939-d5c58768e2bb", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["e2967d3c-238c-40cf-b3d8-89482a502928"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6902-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6902-04", "marketing_start_date": "20161012"}], "brand_name": "Raloxifene hydrochloride", "product_id": "0904-6902_ae852e8a-bdc7-4062-8939-d5c58768e2bb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "0904-6902", "generic_name": "Raloxifene hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA206384", "marketing_category": "ANDA", "marketing_start_date": "20161012", "listing_expiration_date": "20261231"}