MedPath

Myferon 150 Forte

Approved
Approval ID

ed2308e3-5310-41bd-9333-615c26183493

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 20, 2014

Manufacturers
FDA

MARTIN EKWEALOR PHARMACEUTICALS, INC.

DUNS: 624528386

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

IRON SUCROSE, FOLIC ACID, CYANOCOBALAMIN

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code58607-112
Product Classification
G
Generic Name
IRON SUCROSE, FOLIC ACID, CYANOCOBALAMIN
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 20, 2014
FDA Product Classification

INGREDIENTS (13)

CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SHELLACInactive
Code: 46N107B71O
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSInactive
Code: L11K75P92J
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
IRON SUCROSEActive
Quantity: 150 mg in 1 1
Code: FZ7NYF5N8L
Classification: ACTIM
FOLIC ACIDActive
Quantity: 1 mg in 1 1
Code: 935E97BOY8
Classification: ACTIB
CYANOCOBALAMINActive
Quantity: 25 ug in 1 1
Code: P6YC3EG204
Classification: ACTIB
GELATINInactive
Code: 2G86QN327L
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
FERRIC OXIDE REDInactive
Code: 1K09F3G675
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT

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Myferon 150 Forte - FDA Drug Approval Details