Package 59651-341-01

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 59651-341-01
Digits Only 5965134101
Product NDC 59651-341
Product ID 59651-341_a67f1603-a117-4a69-b4f2-ea348425396e
Description

100 TABLET, FILM COATED in 1 BOTTLE (59651-341-01)

Marketing

Marketing Status
Marketed Since 2020-08-12
Brand methocarbamol
Generic methocarbamol
Sample Package No

Linked Drug Pages (1)

Methocarbamol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a67f1603-a117-4a69-b4f2-ea348425396e", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0359651340011"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["f83dd093-ea53-44c1-a40d-682ebc494b62"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-341-01)", "package_ndc": "59651-341-01", "marketing_start_date": "20200812"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59651-341-05)", "package_ndc": "59651-341-05", "marketing_start_date": "20200812"}], "brand_name": "Methocarbamol", "product_id": "59651-341_a67f1603-a117-4a69-b4f2-ea348425396e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "59651-341", "generic_name": "Methocarbamol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA213967", "marketing_category": "ANDA", "marketing_start_date": "20200812", "listing_expiration_date": "20261231"}