Methocarbamol
Methocarbamol Tablets USP
Approved
Approval ID
e89ae224-ed25-4ae7-e053-2a95a90a9c0e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 2, 2024
Manufacturers
FDA
Misemer Pharmaceutical
DUNS: 784121365
Products 1
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 Code0276-0510
Application NumberANDA200958
Product Classification
M
Marketing Category
C73584
G
Generic Name
Methocarbamol
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 2, 2024
FDA Product Classification
INGREDIENTS (1)
METHOCARBAMOLActive
Quantity: 1000 mg in 1 1
Code: 125OD7737X
Classification: ACTIB