Package 68788-8620-1

{"route": ["ORAL"], "spl_id": "8c765672-66b8-44bb-8252-792d539e057b", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["52da1afc-7f1c-4893-ab84-8479dd939951"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8620-1)", "package_ndc": "68788-8620-1", "marketing_start_date": "20240402"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8620-3)", "package_ndc": "68788-8620-3", "marketing_start_date": "20240402"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8620-6)", "package_ndc": "68788-8620-6", "marketing_start_date": "20240402"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8620-9)", "package_ndc": "68788-8620-9", "marketing_start_date": "20240402"}], "brand_name": "Propranolol Hydrochloride", "product_id": "68788-8620_8c765672-66b8-44bb-8252-792d539e057b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-8620", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20240402", "listing_expiration_date": "20261231"}