Package 16571-201-10

{"route": ["ORAL"], "spl_id": "504b1904-033c-4fd8-92c9-41e31154f808", "openfda": {"upc": ["0316571202102"], "unii": ["QTG126297Q"], "rxcui": ["855664", "855906", "855926"], "spl_set_id": ["3330ea92-fc9d-4541-b378-be399b0995d3"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (16571-201-06)", "package_ndc": "16571-201-06", "marketing_start_date": "20080819"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-10)", "package_ndc": "16571-201-10", "marketing_start_date": "20080819"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-11)", "package_ndc": "16571-201-11", "marketing_start_date": "20080819"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-50)", "package_ndc": "16571-201-50", "marketing_start_date": "20080819"}], "brand_name": "Diclofenac Sodium", "product_id": "16571-201_504b1904-033c-4fd8-92c9-41e31154f808", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "16571-201", "generic_name": "Diclofenac Sodium", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA077863", "marketing_category": "ANDA", "marketing_start_date": "20080819", "listing_expiration_date": "20261231"}