Package 59088-724-00

Brand: methocarb 500-ezs

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 59088-724-00
Digits Only 5908872400
Product NDC 59088-724
Description

1 KIT in 1 KIT (59088-724-00) * 100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10)

Marketing

Marketing Status
Marketed Since 2018-10-23
Brand methocarb 500-ezs
Generic methocarbamol
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "b3ca019e-98e0-1007-e053-2a95a90a1690", "openfda": {"upc": ["0731477272217"], "rxcui": ["197943"], "spl_set_id": ["383ce408-1085-43e7-944e-957ff2a9d553"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (59088-724-00)  *  100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10)", "package_ndc": "59088-724-00", "marketing_start_date": "20181023"}], "brand_name": "Methocarb 500-EZS", "product_id": "59088-724_b3ca019e-98e0-1007-e053-2a95a90a1690", "dosage_form": "KIT", "product_ndc": "59088-724", "generic_name": "Methocarbamol", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarb 500-EZS", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20181023", "listing_expiration_date": "20261231"}