Package 80425-0171-1

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 80425-0171-1
Digits Only 8042501711
Product NDC 80425-0171
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0171-1)

Marketing

Marketing Status
Marketed Since 2018-01-15
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": "2a99b1dd-bed2-79f9-e063-6394a90a35f3", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["c9600cc9-7e27-6e19-e053-2995a90ab024"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0171-1)", "package_ndc": "80425-0171-1", "marketing_start_date": "20180115"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0171-2)", "package_ndc": "80425-0171-2", "marketing_start_date": "20180115"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0171-3)", "package_ndc": "80425-0171-3", "marketing_start_date": "20180115"}], "brand_name": "Methocarbamol", "product_id": "80425-0171_2a99b1dd-bed2-79f9-e063-6394a90a35f3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "80425-0171", "generic_name": "Methocarbamol", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20261231"}