Package 58657-603-01

{"route": ["ORAL"], "spl_id": "46b55541-52d5-7213-e063-6294a90affc4", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0358657603014", "0358657603502", "0358657602505", "0358657604509", "0358657602017", "0358657604011"], "unii": ["R5H8897N95"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["733d6e32-ac90-4796-bf25-9d5887c897a5"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (58657-603-01)", "package_ndc": "58657-603-01", "marketing_start_date": "20191122"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (58657-603-50)", "package_ndc": "58657-603-50", "marketing_start_date": "20191122"}], "brand_name": "Labetalol Hydrochloride", "product_id": "58657-603_46b55541-52d5-7213-e063-6294a90affc4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "58657-603", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL", "strength": "200 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20191122", "listing_expiration_date": "20261231"}