Package 0280-0047-36

{"route": ["ORAL"], "spl_id": "45261b62-1428-8c69-e063-6294a90a011f", "openfda": {"unii": ["2968PHW8QP", "8MDF5V39QO"], "rxcui": ["1536470"], "spl_set_id": ["55158e50-0327-2043-e054-00144ff8d46c"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 POUCH in 1 CARTON (0280-0047-36)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-0047-36", "marketing_start_date": "20100302"}], "brand_name": "Alka-Seltzer Heartburn", "product_id": "0280-0047_45261b62-1428-8c69-e063-6294a90a011f", "dosage_form": "TABLET, EFFERVESCENT", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0280-0047", "generic_name": "Anhydrous citric acid, Sodium bicarbonate (heat-treated)", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Heartburn", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "1000 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1940 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100302", "listing_expiration_date": "20261231"}