Package 0904-6731-51

{"route": ["ORAL"], "spl_id": "102f4c28-a2f1-3e69-e063-6394a90af867", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["786dbcd5-f5c2-4491-e053-2991aa0a3437"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6731-51)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0904-6731-51", "marketing_start_date": "20181226"}], "brand_name": "Acetaminophen, Diphenhydramine Hydrochloride", "product_id": "0904-6731_102f4c28-a2f1-3e69-e063-6394a90af867", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0904-6731", "generic_name": "Acetaminophen, Diphenhydramine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen, Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181226", "listing_expiration_date": "20261231"}