Package 80425-0464-1

{"route": ["ORAL"], "spl_id": "29acba15-59d7-ca52-e063-6294a90a272c", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["29ace768-8fef-482b-e063-6394a90aa2ac"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0464-1)", "package_ndc": "80425-0464-1", "marketing_start_date": "20241218"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0464-2)", "package_ndc": "80425-0464-2", "marketing_start_date": "20241218"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0464-3)", "package_ndc": "80425-0464-3", "marketing_start_date": "20241218"}], "brand_name": "Propranolol Hydrochloride", "product_id": "80425-0464_29acba15-59d7-ca52-e063-6294a90a272c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "80425-0464", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20241218", "listing_expiration_date": "20261231"}