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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code60429-118
Application NumberANDA200958
Product Classification
M
Marketing Category
C73584
G
Generic Name
Methocarbamol
Product Specifications
Route of AdministrationORAL
Effective DateMarch 10, 2022
FDA Product Classification
INGREDIENTS (1)
METHOCARBAMOLActive
Quantity: 500 mg in 1 1
Code: 125OD7737X
Classification: ACTIB
Methocarbamol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code60429-119
Application NumberANDA200958
Product Classification
M
Marketing Category
C73584
G
Generic Name
Methocarbamol
Product Specifications
Route of AdministrationORAL
Effective DateMarch 10, 2022
FDA Product Classification
INGREDIENTS (1)
METHOCARBAMOLActive
Quantity: 750 mg in 1 1
Code: 125OD7737X
Classification: ACTIB