Package 76420-258-90

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 76420-258-90
Digits Only 7642025890
Product NDC 76420-258
Description

90 TABLET in 1 BOTTLE (76420-258-90)

Marketing

Marketing Status
Marketed Since 2019-08-15
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": "1ad285fe-2e2c-5b7a-e063-6294a90aaad0", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["5a9b1104-4c9a-4c8c-9e24-719a7b3a89d7"], "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 (76420-258-10)", "package_ndc": "76420-258-10", "marketing_start_date": "20190815"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-258-30)", "package_ndc": "76420-258-30", "marketing_start_date": "20190815"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-258-60)", "package_ndc": "76420-258-60", "marketing_start_date": "20190815"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-258-90)", "package_ndc": "76420-258-90", "marketing_start_date": "20190815"}], "brand_name": "Methocarbamol", "product_id": "76420-258_1ad285fe-2e2c-5b7a-e063-6294a90aaad0", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-258", "generic_name": "methocarbamol", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20190815", "listing_expiration_date": "20261231"}