Package 51655-205-20

{"route": ["ORAL"], "spl_id": "48d29482-0b02-e65f-e063-6394a90a865b", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["f2b4ed5f-3489-9ee4-e053-2995a90a25f0"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-20)", "package_ndc": "51655-205-20", "marketing_start_date": "20230108"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-52)", "package_ndc": "51655-205-52", "marketing_start_date": "20230413"}], "brand_name": "Methocarbamol", "product_id": "51655-205_48d29482-0b02-e65f-e063-6394a90a865b", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "51655-205", "generic_name": "Methocarbamol Tablets", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_start_date": "20230108", "listing_expiration_date": "20271231"}