Package 0093-7290-56

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-7290-56
Digits Only 0093729056
Product NDC 0093-7290
Product ID 0093-7290_3641edbc-4bae-45d0-8afb-8db02f401f66
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-7290-56)

Marketing

Marketing Status
Marketed Since 2014-03-28
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": "3641edbc-4bae-45d0-8afb-8db02f401f66", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["e6be5b1d-757d-4bab-ad6a-c421960a104d"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-7290-01)", "package_ndc": "0093-7290-01", "marketing_start_date": "20140328"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-7290-56)", "package_ndc": "0093-7290-56", "marketing_start_date": "20140328"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "0093-7290_3641edbc-4bae-45d0-8afb-8db02f401f66", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "0093-7290", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA078193", "marketing_category": "ANDA", "marketing_start_date": "20140328", "listing_expiration_date": "20261231"}