Package 68788-8880-3
Brand: methocarbamol
Generic: methocarbamolPackage Facts
Identity
Package NDC
68788-8880-3
Digits Only
6878888803
Product NDC
68788-8880
Description
30 TABLET, FILM COATED in 1 BOTTLE (68788-8880-3)
Marketing
Marketing Status
Brand
methocarbamol
Generic
methocarbamol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5a48be27-5069-40f3-85de-86f248ae232f", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["5a48be27-5069-40f3-85de-86f248ae232f"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8880-3)", "package_ndc": "68788-8880-3", "marketing_start_date": "20250602"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8880-6)", "package_ndc": "68788-8880-6", "marketing_start_date": "20250602"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8880-9)", "package_ndc": "68788-8880-9", "marketing_start_date": "20250602"}], "brand_name": "METHOCARBAMOL", "product_id": "68788-8880_5a48be27-5069-40f3-85de-86f248ae232f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-8880", "generic_name": "METHOCARBAMOL", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHOCARBAMOL", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA203550", "marketing_category": "ANDA", "marketing_start_date": "20250602", "listing_expiration_date": "20261231"}