Methocarbamol
Methocarbamol Tablets 750mg
Approved
Approval ID
a88a6c84-b55a-4b6b-ac01-554079f6e304
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 1, 2022
Manufacturers
FDA
Key Therapeutics
DUNS: 080318791
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 Code70868-901
Application NumberANDA040489
Product Classification
M
Marketing Category
C73584
G
Generic Name
methocarbamol
Product Specifications
Route of AdministrationORAL
Effective DateMarch 31, 2022
FDA Product Classification
INGREDIENTS (8)
MethocarbamolActive
Quantity: 750 mg in 1 1
Code: 125OD7737X
Classification: ACTIB
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
Povidone K90Inactive
Code: RDH86HJV5Z
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT
Stearic AcidInactive
Code: 4ELV7Z65AP
Classification: IACT