Package 31722-046-31

{"route": ["ORAL"], "spl_id": "2d0e1b57-79e2-61da-e063-6394a90a214e", "openfda": {"upc": ["0331722046329"], "unii": ["L4D5UA6CB4"], "rxcui": ["859063"], "spl_set_id": ["9261a9d6-f772-41a2-ac99-8608c04c355b"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POWDER, FOR SOLUTION in 1 PACKET (31722-046-31)", "package_ndc": "31722-046-31", "marketing_start_date": "20220304"}, {"sample": false, "description": "9 POWDER, FOR SOLUTION in 1 CARTON (31722-046-32)", "package_ndc": "31722-046-32", "marketing_start_date": "20220304"}], "brand_name": "Diclofenac potassium", "product_id": "31722-046_2d0e1b57-79e2-61da-e063-6394a90a214e", "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": "31722-046", "generic_name": "Diclofenac potassium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215375", "marketing_category": "ANDA", "marketing_start_date": "20220304", "listing_expiration_date": "20261231"}