Package 67877-626-05

{"route": ["ORAL"], "spl_id": "5107e958-bc99-4832-931e-4c47e25ec6eb", "openfda": {"nui": ["N0000000151", "N0000175784", "N0000000160", "M0001335", "N0000175722"], "upc": ["0367877626901", "0367877626062"], "unii": ["5QZO15J2Z8", "WK2XYI10QM"], "rxcui": ["1100066"], "spl_set_id": ["4493d4cd-ca8e-4b0a-9b65-b75e55bf8b9e"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]", "Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (67877-626-01)", "package_ndc": "67877-626-01", "marketing_start_date": "20210804"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-626-05)", "package_ndc": "67877-626-05", "marketing_start_date": "20210804"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (67877-626-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-626-06", "marketing_start_date": "20210804"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (67877-626-90)", "package_ndc": "67877-626-90", "marketing_start_date": "20210804"}], "brand_name": "Ibuprofen and famotidine", "product_id": "67877-626_5107e958-bc99-4832-931e-4c47e25ec6eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67877-626", "generic_name": "Ibuprofen and famotidine", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen and famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "26.6 mg/1"}, {"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA211890", "marketing_category": "ANDA", "marketing_start_date": "20210804", "listing_expiration_date": "20261231"}