Package 60687-266-21

Brand: raloxifene hydrochloride

Generic: raloxifene
NDC Package

Package Facts

Identity

Package NDC 60687-266-21
Digits Only 6068726621
Product NDC 60687-266
Product ID 60687-266_18588c41-973d-4ebc-e063-6294a90a5eed
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-266-21) / 1 TABLET in 1 BLISTER PACK (60687-266-11)

Marketing

Marketing Status
Marketed Since 2016-11-09
Brand raloxifene hydrochloride
Generic raloxifene
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": "18588c41-973d-4ebc-e063-6294a90a5eed", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["f5c25553-1546-451d-8069-c0f484c47741"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-266-21)  / 1 TABLET in 1 BLISTER PACK (60687-266-11)", "package_ndc": "60687-266-21", "marketing_start_date": "20161109"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "60687-266_18588c41-973d-4ebc-e063-6294a90a5eed", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "60687-266", "generic_name": "Raloxifene", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090842", "marketing_category": "ANDA", "marketing_start_date": "20161109", "listing_expiration_date": "20261231"}