Package 51672-4240-6

{"route": ["ORAL"], "spl_id": "24354f73-c3f7-12fa-e063-6294a90ac338", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["859063"], "spl_set_id": ["68a926a2-b818-420f-9c9a-fd91dc5a8f36"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 PACKET in 1 CARTON (51672-4240-6)  / 1 POWDER, FOR SOLUTION in 1 PACKET (51672-4240-8)", "package_ndc": "51672-4240-6", "marketing_start_date": "20240624"}], "brand_name": "Diclofenac Potassium", "product_id": "51672-4240_24354f73-c3f7-12fa-e063-6294a90ac338", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51672-4240", "generic_name": "Diclofenac Potassium", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA218011", "marketing_category": "ANDA", "marketing_start_date": "20240624", "listing_expiration_date": "20261231"}