Package 10135-722-01

{"route": ["ORAL"], "spl_id": "441fa8ee-c4b7-d58f-e063-6394a90a3229", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["d2e38ac9-1cf3-14ca-e053-2a95a90a8522"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10135-722-01)", "package_ndc": "10135-722-01", "marketing_start_date": "20211209"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (10135-722-05)", "package_ndc": "10135-722-05", "marketing_start_date": "20211209"}], "brand_name": "Methocarbamol Tablets, USP, 500 mg", "product_id": "10135-722_441fa8ee-c4b7-d58f-e063-6394a90a3229", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "10135-722", "generic_name": "Methocarbamol", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol Tablets, USP, 500 mg", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA212623", "marketing_category": "ANDA", "marketing_start_date": "20211209", "listing_expiration_date": "20261231"}