Package 69676-0063-2

{"route": ["ORAL"], "spl_id": "2e9472c4-b466-e4fd-e063-6394a90ad2f6", "openfda": {"upc": ["0850015736148"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["d82cf6f3-a291-ca2b-e053-2a95a90a6de1"], "manufacturer_name": ["Genexa Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69676-0063-2)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "69676-0063-2", "marketing_start_date": "20220217"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69676-0063-5)  / 50 TABLET, COATED in 1 BOTTLE", "package_ndc": "69676-0063-5", "marketing_start_date": "20220217"}], "brand_name": "Genexa Acetaminophen PM Extra Strength", "product_id": "69676-0063_2e9472c4-b466-e4fd-e063-6394a90ad2f6", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69676-0063", "generic_name": "Acetaminophen", "labeler_name": "Genexa Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Genexa Acetaminophen PM", "brand_name_suffix": "Extra Strength", "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": "20220217", "listing_expiration_date": "20261231"}