Package 63561-0174-1

{"route": ["ORAL"], "spl_id": "35c0e9af-ba8b-0416-e063-6294a90a87f6", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0363561017352", "0363561017451", "0363561017314"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["70c5342c-9597-4fe6-863c-f8ae4adc063a"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Granulation Technology, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (63561-0174-1)", "package_ndc": "63561-0174-1", "marketing_start_date": "20250610"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63561-0174-5)", "package_ndc": "63561-0174-5", "marketing_start_date": "20250610"}], "brand_name": "Methocarbamol Tablets, USP, 750 mg", "product_id": "63561-0174_35c0e9af-ba8b-0416-e063-6294a90a87f6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "63561-0174", "generic_name": "Methocarbamol", "labeler_name": "Granulation Technology, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol Tablets, USP, 750 mg", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA212623", "marketing_category": "ANDA", "marketing_start_date": "20250610", "listing_expiration_date": "20261231"}