Package 68210-5053-1

{"route": ["ORAL"], "spl_id": "474d264f-eafa-e891-e063-6394a90a6f40", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["3afc88c7-388a-dbd9-e063-6294a90a4faf"], "manufacturer_name": ["Prodose, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 CARTON (68210-5053-1)  / 3000 CAPSULE, LIQUID FILLED in 1 POUCH", "package_ndc": "68210-5053-1", "marketing_start_date": "20250729"}], "brand_name": "Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride", "product_id": "68210-5053_474d264f-eafa-e891-e063-6394a90a6f40", "dosage_form": "CAPSULE, LIQUID FILLED", "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": "68210-5053", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride", "labeler_name": "Prodose, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride", "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": "20250729", "listing_expiration_date": "20271231"}