Package 43063-848-30

{"route": ["ORAL"], "spl_id": "2fc3b270-b101-5a08-e063-6394a90a7fd2", "openfda": {"upc": ["0343063848210"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["08e41a9d-644c-4ac6-aba3-38d7c3f36d36"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-21)", "package_ndc": "43063-848-21", "marketing_start_date": "20180412"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-30)", "package_ndc": "43063-848-30", "marketing_start_date": "20180412"}], "brand_name": "Diclofenac Potassium", "product_id": "43063-848_2fc3b270-b101-5a08-e063-6394a90a7fd2", "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": "43063-848", "generic_name": "Diclofenac Potassium", "labeler_name": "PD-Rx 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"}