Package 76420-894-90
Brand: methocarbamol
Generic: methocarbamol tabletsPackage Facts
Identity
Package NDC
76420-894-90
Digits Only
7642089490
Product NDC
76420-894
Description
90 TABLET, COATED in 1 BOTTLE (76420-894-90)
Marketing
Marketing Status
Brand
methocarbamol
Generic
methocarbamol tablets
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cbe9e1b-d4dc-de70-e063-6394a90a18b8", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["edbcf8c6-0df8-4e72-885b-16d378f06c7b"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (76420-894-01)", "package_ndc": "76420-894-01", "marketing_start_date": "20250128"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (76420-894-05)", "package_ndc": "76420-894-05", "marketing_start_date": "20250128"}, {"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (76420-894-12)", "package_ndc": "76420-894-12", "marketing_start_date": "20250128"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (76420-894-30)", "package_ndc": "76420-894-30", "marketing_start_date": "20250128"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (76420-894-60)", "package_ndc": "76420-894-60", "marketing_start_date": "20250128"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (76420-894-90)", "package_ndc": "76420-894-90", "marketing_start_date": "20250128"}], "brand_name": "Methocarbamol", "product_id": "76420-894_2cbe9e1b-d4dc-de70-e063-6394a90a18b8", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-894", "generic_name": "Methocarbamol Tablets", "labeler_name": "Asclemed USA, Inc.", "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": "20180702", "listing_expiration_date": "20261231"}