FDA.reportPublic FDA data

iFerex 150 Forte

Manufacturer
Nnodum Pharmaceuticals | Contract Pharmacal Corporation
Effective date
2023-12-28
Label type
DIETARY SUPPLEMENT
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:16:38

Label at a glance#

ProductiFerex 150 Forte
Active ingredientIRON, CYANOCOBALAMIN, FOLIC ACID
Label structure6 sections

Dosage and administration

Adults: iFerex 150 Forte is to be taken one capsule once a day or as prescribed by a physician.

Label contents#

Full prescribing information#

STATEMENT OF IDENTITY SECTION

Polysaccharide Iron Complex

Hematinic Capsules

NDC 63044-0198-01

WARNINGS:

WARNINGS SECTION

Folic acid alone is improper therapy fin the treatment of pernicious anemia and other megaloblastic anemias where vitamin B-12 is deficient.

PRECAUTIONS:

PRECAUTIONS SECTION

Folic acid in doses above 0..1 mg - 0..4 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations remain progressive.

Pediatric Use Safety and effectiveness in pediatric patients has not been established.

SAFE HANDLING WARNING:

SAFE HANDLING WARNING SECTION

Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6.

Keep this products out of the reach of children. In case of accidental overdose, call a doctor or poison control immediately.

DOSAGE AND ADMINISTRATION:

DOSAGE & ADMINISTRATION SECTION

Adults: iFerex 150 Forte is to be taken one capsule once a day or as prescribed by a physician.

iFerex 150 Forte PACKAGE LABEL/PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

iFerex 150 Forte  10 x 10 Unit Dose Capsules

iFerex 150 Forte 198 BoxiFerex 150 Forte 198 Box

iFerex 150 Forte 100 Capsules

iFerex 150 Forte 198 BotliFerex 150 Forte 198 Botl

res

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63044-198-01EA - Each63044-198678062b7-0144-4fe0-be24-dd0cf830f9ed12012-07-24
63044-198-62EA - Each63044-19846b66e8f-94af-41e2-b62f-5e32fdfd0f2712022-01-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CYANOCOBALAMINACTIVE INGREDIENTP6YC3EG2043
FOLIC ACIDACTIVE INGREDIENT935E97BOY83
IRONACTIVE INGREDIENTE1UOL152H73
CYANOCOBALAMINACTIVE MOIETYP6YC3EG2043
FOLIC ACIDACTIVE MOIETY935E97BOY83
IRONACTIVE MOIETYE1UOL152H73

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63044-19863044-198-01, 63044-198-62

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
IRONE1UOL152H7ACTIB
CYANOCOBALAMINP6YC3EG204ACTIB
FOLIC ACID935E97BOY8ACTIB
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
GELATIN2G86QN327LIACT
MAGNESIUM STEARATE70097M6I30IACT
D&C RED NO. 28767IP0Y5NHIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FD&C RED NO. 3PN2ZH5LOQYIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C YELLOW NO. 1035SW5USQ3GIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a918714f-b82f-43c1-b8fe-fcdb7fc9ae0eb27b10a5-b539-4ebb-af3f-d35439eca70c2018-04-25Warnings, Adverse reactionsExact identifier
spl set id: b27b10a5-b539-4ebb-af3f-d35439eca70c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.