Package 80136-384-24

{"route": ["ORAL"], "spl_id": "dc8efd7a-1632-46ea-8d21-9b443ff6081c", "openfda": {"nui": ["N0000010282"], "unii": ["92RU3N3Y1O", "77TI35393C"], "rxcui": ["978001"], "spl_set_id": ["d106d8e5-cdbb-4f90-8456-e692ffe7f4e6"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["NORTHEAST PHARMA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (80136-384-24)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "80136-384-24", "marketing_start_date": "20211027"}], "brand_name": "Loperamide Hydrochloride and Simethicone", "product_id": "80136-384_dc8efd7a-1632-46ea-8d21-9b443ff6081c", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]", "Skin Barrier Activity [PE]"], "product_ndc": "80136-384", "generic_name": "Loperamide Hydrochloride and Simethicone", "labeler_name": "NORTHEAST PHARMA", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride and Simethicone", "active_ingredients": [{"name": "DIMETHICONE", "strength": "125 mg/1"}, {"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA211059", "marketing_category": "ANDA", "marketing_start_date": "20211027", "listing_expiration_date": "20261231"}