Package 70518-4469-0

{"route": ["ORAL"], "spl_id": "44e417ef-3166-675d-e063-6394a90a7615", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["56379133-cd11-4dff-b511-7cdfc9a360ca"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4469-0)", "package_ndc": "70518-4469-0", "marketing_start_date": "20250908"}, {"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (70518-4469-1)", "package_ndc": "70518-4469-1", "marketing_start_date": "20250908"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4469-2)", "package_ndc": "70518-4469-2", "marketing_start_date": "20251130"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-4469_44e417ef-3166-675d-e063-6394a90a7615", "dosage_form": "TABLET, COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4469", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA212654", "marketing_category": "ANDA", "marketing_start_date": "20250908", "listing_expiration_date": "20261231"}