Package 76420-898-90
Brand: metaxalone
Generic: metaxalonePackage Facts
Identity
Package NDC
76420-898-90
Digits Only
7642089890
Product NDC
76420-898
Description
90 TABLET in 1 BOTTLE (76420-898-90)
Marketing
Marketing Status
Brand
metaxalone
Generic
metaxalone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3507d3aa-6c7f-962d-e063-6294a90ae333", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["1NMA9J598Y"], "rxcui": ["351254"], "spl_set_id": ["f4a0e910-2b20-46d4-b49e-21fb15925b58"], "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 in 1 BOTTLE (76420-898-01)", "package_ndc": "76420-898-01", "marketing_start_date": "20250110"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (76420-898-12)", "package_ndc": "76420-898-12", "marketing_start_date": "20250513"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (76420-898-15)", "package_ndc": "76420-898-15", "marketing_start_date": "20250110"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-898-20)", "package_ndc": "76420-898-20", "marketing_start_date": "20250110"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-898-30)", "package_ndc": "76420-898-30", "marketing_start_date": "20250110"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-898-60)", "package_ndc": "76420-898-60", "marketing_start_date": "20250110"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-898-90)", "package_ndc": "76420-898-90", "marketing_start_date": "20250110"}], "brand_name": "Metaxalone", "product_id": "76420-898_3507d3aa-6c7f-962d-e063-6294a90ae333", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-898", "generic_name": "Metaxalone", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metaxalone", "active_ingredients": [{"name": "METAXALONE", "strength": "800 mg/1"}], "application_number": "ANDA203695", "marketing_category": "ANDA", "marketing_start_date": "20170619", "listing_expiration_date": "20261231"}