Package 71610-053-60

Brand: raloxifene hydrochloride

Generic: raloxifene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-053-60
Digits Only 7161005360
Product NDC 71610-053
Product ID 71610-053_29e0719a-c1c4-429b-8544-f1efe06c33fd
Description

90 TABLET, FILM COATED in 1 BOTTLE (71610-053-60)

Marketing

Marketing Status
Marketed Since 2018-04-26
Brand raloxifene hydrochloride
Generic raloxifene hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "29e0719a-c1c4-429b-8544-f1efe06c33fd", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["6fd63a06-5bc5-4c50-9b85-b09c89100b80"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-053-60)", "package_ndc": "71610-053-60", "marketing_start_date": "20180426"}], "brand_name": "Raloxifene hydrochloride", "product_id": "71610-053_29e0719a-c1c4-429b-8544-f1efe06c33fd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "71610-053", "generic_name": "Raloxifene hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}