Package 53489-479-10

Brand: sulindac

Generic: sulindac
NDC Package

Package Facts

Identity

Package NDC 53489-479-10
Digits Only 5348947910
Product NDC 53489-479
Description

1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10)

Marketing

Marketing Status
Marketed Since 2009-09-04
Brand sulindac
Generic sulindac
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2524fd49-5789-e388-e063-6394a90a2c9b", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0353489479011", "0353489478014"], "unii": ["184SNS8VUH"], "rxcui": ["198238", "198239"], "spl_set_id": ["a47e4259-d44b-4b7b-b517-841cb6840982"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01)", "package_ndc": "53489-479-01", "marketing_start_date": "20090904"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02)", "package_ndc": "53489-479-02", "marketing_start_date": "20090904"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03)", "package_ndc": "53489-479-03", "marketing_start_date": "20090904"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05)", "package_ndc": "53489-479-05", "marketing_start_date": "20090904"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06)", "package_ndc": "53489-479-06", "marketing_start_date": "20090904"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10)", "package_ndc": "53489-479-10", "marketing_start_date": "20090904"}], "brand_name": "SULINDAC", "product_id": "53489-479_2524fd49-5789-e388-e063-6394a90a2c9b", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "53489-479", "generic_name": "sulindac", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SULINDAC", "active_ingredients": [{"name": "SULINDAC", "strength": "200 mg/1"}], "application_number": "ANDA072051", "marketing_category": "ANDA", "marketing_start_date": "20090904", "listing_expiration_date": "20261231"}