Package 69848-014-05

{"route": ["ORAL"], "spl_id": "4690f59f-4424-6231-e063-6294a90a8ca7", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["8c9f68e3-fedc-6457-e053-2995a90a045a"], "manufacturer_name": ["Granules USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (69848-014-02)", "package_ndc": "69848-014-02", "marketing_start_date": "20190701"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (69848-014-05)", "package_ndc": "69848-014-05", "marketing_start_date": "20190701"}, {"sample": false, "description": "150 TABLET in 1 BOTTLE (69848-014-15)", "package_ndc": "69848-014-15", "marketing_start_date": "20190701"}], "brand_name": "Acetaminophen Diphenhydramine HCl", "product_id": "69848-014_4690f59f-4424-6231-e063-6294a90a8ca7", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69848-014", "generic_name": "Acetaminophen Diphenhydramine HCl", "labeler_name": "Granules USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Diphenhydramine HCl", "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": "20190701", "listing_expiration_date": "20261231"}