Package 71335-2434-4

{"route": ["ORAL"], "spl_id": "41d78266-20c3-e397-e063-6294a90a1c20", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["dafa7411-2857-4f5a-a587-4367cfbe2bfa"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2434-1)", "package_ndc": "71335-2434-1", "marketing_start_date": "20240715"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2434-2)", "package_ndc": "71335-2434-2", "marketing_start_date": "20240715"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-2434-3)", "package_ndc": "71335-2434-3", "marketing_start_date": "20240715"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2434-4)", "package_ndc": "71335-2434-4", "marketing_start_date": "20240715"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-2434-5)", "package_ndc": "71335-2434-5", "marketing_start_date": "20240715"}], "brand_name": "Labetalol Hydrochloride", "product_id": "71335-2434_41d78266-20c3-e397-e063-6294a90a1c20", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2434", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20210527", "listing_expiration_date": "20261231"}