Package 41520-138-05

{"route": ["ORAL"], "spl_id": "2489b22e-7d05-8fdb-e063-6394a90acdb4", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1094538"], "spl_set_id": ["d2dcbc7c-e66c-4922-83df-c706a37bf334"], "manufacturer_name": ["American Sales Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (41520-138-05)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "41520-138-05", "marketing_start_date": "20110901"}], "brand_name": "Cold Multi-Symptom Daytime", "product_id": "41520-138_2489b22e-7d05-8fdb-e063-6394a90acdb4", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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": "41520-138", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "American Sales Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold Multi-Symptom Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110901", "listing_expiration_date": "20261231"}