Package 68788-8822-4

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 68788-8822-4
Digits Only 6878888224
Product NDC 68788-8822
Description

40 TABLET in 1 BOTTLE (68788-8822-4)

Marketing

Marketing Status
Marketed Since 2025-02-10
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": "eed9ebd1-c243-4e82-bf4e-5fec370e722e", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["eed9ebd1-c243-4e82-bf4e-5fec370e722e"], "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": "100 TABLET in 1 BOTTLE (68788-8822-1)", "package_ndc": "68788-8822-1", "marketing_start_date": "20250210"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8822-2)", "package_ndc": "68788-8822-2", "marketing_start_date": "20250210"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8822-3)", "package_ndc": "68788-8822-3", "marketing_start_date": "20250210"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68788-8822-4)", "package_ndc": "68788-8822-4", "marketing_start_date": "20250210"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8822-6)", "package_ndc": "68788-8822-6", "marketing_start_date": "20250210"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-8822-8)", "package_ndc": "68788-8822-8", "marketing_start_date": "20250210"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8822-9)", "package_ndc": "68788-8822-9", "marketing_start_date": "20250210"}], "brand_name": "Methocarbamol", "product_id": "68788-8822_eed9ebd1-c243-4e82-bf4e-5fec370e722e", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-8822", "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": "ANDA090200", "marketing_category": "ANDA", "marketing_start_date": "20250210", "listing_expiration_date": "20261231"}