Package 48201-001-12

{"route": ["ORAL"], "spl_id": "42404180-fa1a-fcf6-e063-6394a90a281f", "openfda": {"upc": ["0348201018142"], "unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1193292"], "spl_set_id": ["4af8a566-5251-4d46-8692-87a3a0748334"], "manufacturer_name": ["GRANDALL DISTRIBUTING, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CAPSULE, GELATIN COATED in 1 BOX (48201-001-12)", "package_ndc": "48201-001-12", "marketing_start_date": "20150430"}], "brand_name": "Sanaflu Xtra", "product_id": "48201-001_42404180-fa1a-fcf6-e063-6394a90a281f", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "48201-001", "generic_name": "ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "GRANDALL DISTRIBUTING, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sanaflu Xtra", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "2 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150430", "listing_expiration_date": "20261231"}