Package 76420-891-06

{"route": ["ORAL"], "spl_id": "2abbd7c9-640f-d0cb-e063-6294a90a23f0", "openfda": {"nui": ["N0000000151", "N0000175784", "N0000000160", "M0001335", "N0000175722"], "unii": ["5QZO15J2Z8", "WK2XYI10QM"], "rxcui": ["1100066"], "spl_set_id": ["41123df3-97ac-4c4f-9a89-f76ec03898bb"], "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": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-891-01)", "package_ndc": "76420-891-01", "marketing_start_date": "20250102"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76420-891-05)", "package_ndc": "76420-891-05", "marketing_start_date": "20250102"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (76420-891-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "76420-891-06", "marketing_start_date": "20250102"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-891-30)", "package_ndc": "76420-891-30", "marketing_start_date": "20250102"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-891-60)", "package_ndc": "76420-891-60", "marketing_start_date": "20250102"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-891-90)", "package_ndc": "76420-891-90", "marketing_start_date": "20250102"}], "brand_name": "Ibuprofen and famotidine", "product_id": "76420-891_2abbd7c9-640f-d0cb-e063-6294a90a23f0", "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": "76420-891", "generic_name": "Ibuprofen and famotidine", "labeler_name": "Asclemed USA, Inc.", "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"}