Package 51672-2144-1

{"route": ["ORAL"], "spl_id": "3962343e-c4c0-0b67-e063-6294a90afb17", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0351672214487"], "unii": ["WK2XYI10QM"], "rxcui": ["197803"], "spl_set_id": ["6cf3328b-da8f-4f6b-8237-16a4d6b9c833"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-2144-1)  / 240 mL in 1 BOTTLE", "package_ndc": "51672-2144-1", "marketing_start_date": "20220721"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-2144-8)  / 120 mL in 1 BOTTLE", "package_ndc": "51672-2144-8", "marketing_start_date": "20220721"}], "brand_name": "Ibuprofen", "product_id": "51672-2144_3962343e-c4c0-0b67-e063-6294a90afb17", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51672-2144", "generic_name": "Ibuprofen", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "100 mg/5mL"}], "application_number": "ANDA209207", "marketing_category": "ANDA", "marketing_start_date": "20220721", "listing_expiration_date": "20261231"}