Menatrol
Menatrol
Approved
Approval ID
0a100e7d-3a8d-2d8b-e063-6394a90a3203
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 18, 2023
Manufacturers
FDA
PureTek Corporation
DUNS: 785961046
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Folate, Multivitamin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code59088-156
Product Classification
G
Generic Name
Folate, Multivitamin
Product Specifications
Route of AdministrationORAL
Effective DateDecember 18, 2023
FDA Product Classification
INGREDIENTS (9)
PYRIDOXINE HYDROCHLORIDEActive
Quantity: 1.5 mg in 1 1
Code: 68Y4CF58BV
Classification: ACTIB
.ALPHA.-TOCOPHEROL ACETATE, DL-Inactive
Code: WR1WPI7EW8
Classification: IACT
CHOLECALCIFEROLActive
Quantity: 600 [iU] in 1 1
Code: 1C6V77QF41
Classification: ACTIB
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
LEVOMEFOLATE CALCIUMActive
Quantity: 1000 ug in 1 1
Code: A9R10K3F2F
Classification: ACTIB
MAGNESIUM OXIDEActive
Quantity: 100 mg in 1 1
Code: 3A3U0GI71G
Classification: ACTIB
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
RHUBARBActive
Quantity: 4 mg in 1 1
Code: G280W4MW6E
Classification: ACTIB
CALCIUM CARBONATEActive
Quantity: 220 mg in 1 1
Code: H0G9379FGK
Classification: ACTIM