Package 72789-423-30

{"route": ["ORAL"], "spl_id": "3cf830d5-c282-64d5-e063-6294a90af427", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["49d09308-74b0-4f9a-9c03-37234b5ee3a3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-423-30)", "package_ndc": "72789-423-30", "marketing_start_date": "20240712"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-423-60)", "package_ndc": "72789-423-60", "marketing_start_date": "20241223"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-423-90)", "package_ndc": "72789-423-90", "marketing_start_date": "20250603"}], "brand_name": "Propranolol Hydrochloride", "product_id": "72789-423_3cf830d5-c282-64d5-e063-6294a90af427", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72789-423", "generic_name": "Propranolol Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}