Package 70518-3993-0

{"route": ["ORAL"], "spl_id": "3f8fc907-586d-8e31-e063-6294a90a40a0", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["5101b8dd-6148-465c-9bba-0209ce823fe5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-0)", "package_ndc": "70518-3993-0", "marketing_start_date": "20240124"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-1)", "package_ndc": "70518-3993-1", "marketing_start_date": "20240124"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-2)", "package_ndc": "70518-3993-2", "marketing_start_date": "20250120"}], "brand_name": "Labetalol Hydrochloride", "product_id": "70518-3993_3f8fc907-586d-8e31-e063-6294a90a40a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3993", "generic_name": "Labetalol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20240124", "listing_expiration_date": "20261231"}