Package 66267-070-60

{"route": ["ORAL"], "spl_id": "1f98d6d5-cf08-a2bf-e063-6294a90a370b", "openfda": {"upc": ["0366267070904"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["3da9e463-1b2f-54c0-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (66267-070-30)", "package_ndc": "66267-070-30", "marketing_start_date": "20160929"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (66267-070-60)", "package_ndc": "66267-070-60", "marketing_start_date": "20160929"}], "brand_name": "Diclofenac Potassium", "product_id": "66267-070_1f98d6d5-cf08-a2bf-e063-6294a90a370b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "66267-070", "generic_name": "Diclofenac Potassium", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075219", "marketing_category": "ANDA", "marketing_start_date": "19980811", "listing_expiration_date": "20261231"}