Package 16714-213-01

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-213-01
Digits Only 1671421301
Product NDC 16714-213
Product ID 16714-213_145e48c3-0ef5-41f7-adc2-ab0a7ca89d87
Description

30 TABLET, FILM COATED in 1 BOTTLE (16714-213-01)

Marketing

Marketing Status
Marketed Since 2015-08-28
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": "145e48c3-0ef5-41f7-adc2-ab0a7ca89d87", "openfda": {"upc": ["0316714213019"], "unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["0f7d1f81-374f-4ad5-aea0-2f97abbe1dbf"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-213-01)", "package_ndc": "16714-213-01", "marketing_start_date": "20150828"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-213-02)", "package_ndc": "16714-213-02", "marketing_start_date": "20150828"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16714-213-03)", "package_ndc": "16714-213-03", "marketing_start_date": "20150828"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "16714-213_145e48c3-0ef5-41f7-adc2-ab0a7ca89d87", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "16714-213", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204310", "marketing_category": "ANDA", "marketing_start_date": "20150828", "listing_expiration_date": "20261231"}