Package 43063-972-30
Brand: nabumetone
Generic: nabumetonePackage Facts
Identity
Package NDC
43063-972-30
Digits Only
4306397230
Product NDC
43063-972
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)
Marketing
Marketing Status
Brand
nabumetone
Generic
nabumetone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36c31358-008c-bd73-e063-6294a90a06cf", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0343063972205"], "unii": ["LW0TIW155Z"], "rxcui": ["311892"], "spl_set_id": ["8f3c1b1d-2765-4cb5-92df-044b99339c92"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-20)", "package_ndc": "43063-972-20", "marketing_start_date": "20190422"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)", "package_ndc": "43063-972-30", "marketing_start_date": "20190710"}], "brand_name": "Nabumetone", "product_id": "43063-972_36c31358-008c-bd73-e063-6294a90a06cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43063-972", "generic_name": "Nabumetone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nabumetone", "active_ingredients": [{"name": "NABUMETONE", "strength": "500 mg/1"}], "application_number": "ANDA078671", "marketing_category": "ANDA", "marketing_start_date": "20190306", "listing_expiration_date": "20261231"}