Package 50090-6774-0

{"route": ["ORAL"], "spl_id": "bf2e3b2f-4973-4e8a-9131-779dc6e8fbd9", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["1a71964e-e6fa-443e-bfdd-f8852f8cf29e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-6774-0)", "package_ndc": "50090-6774-0", "marketing_start_date": "20231024"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6774-1)", "package_ndc": "50090-6774-1", "marketing_start_date": "20231024"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "50090-6774_bf2e3b2f-4973-4e8a-9131-779dc6e8fbd9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-6774", "generic_name": "Labetalol Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LABETALOL HYDROCHLORIDE", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA211953", "marketing_category": "ANDA", "marketing_start_date": "20210818", "listing_expiration_date": "20261231"}