Methocarbamol
Methocarbamol Tablets USP
Approved
Approval ID
58f867fd-cad0-4bef-9bd6-9c401bda2120
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 10, 2022
Manufacturers
FDA
Golden State Medical Supply, Inc.
DUNS: 603184490
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Methocarbamol
PRODUCT DETAILS
NDC Product Code60429-118
Application NumberANDA200958
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateMarch 10, 2022
Generic NameMethocarbamol
INGREDIENTS (1)
METHOCARBAMOLActive
Quantity: 500 mg in 1 1
Code: 125OD7737X
Classification: ACTIB
Methocarbamol
PRODUCT DETAILS
NDC Product Code60429-119
Application NumberANDA200958
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateMarch 10, 2022
Generic NameMethocarbamol
INGREDIENTS (1)
METHOCARBAMOLActive
Quantity: 750 mg in 1 1
Code: 125OD7737X
Classification: ACTIB