FerraPlus 90

Name: FerraPlus 90

FerraPlus 90 Tablets with 90 mg Carbonyl Iron

Rx Only

Indications and Usage for FerraPlus 90

FerraPlus 90 is indicated for the treatment of all anemias that are responsive to oral iron therapy. These include: hypochromic anemia associated with pregnancy, chronic and/or acute blood loss, metabolic disease, post-surgical convalescence, and dietary needs.

Precautions

General

Take 2 hours after meals. Do not exceed recommended dose. Discontinue use if symptoms of intolerance appear. The type of anemia and underlying cause or causes should be determined before starting therapy with FerraPlus 90 tablets. Ensure Hgb, Hct, reticulocyte count are determined before starting therapy and periodically thereafter during prolonged treatment. Periodically review therapy to determine if it needs to be continued without change or if a dose change is indicated.

Folic Acid

Folic acid in doses above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations remain progressive. Pernicious anemia should be excluded before using these products since folic acid may mask the symptoms of pernicious anemia.

Pediatric Use

Safety and effectiveness in pediatric patients have not been established.

Geriatric Use

Dosing for elderly patients should be cautious. Due to the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy, dosing should start at the lower end of the dosing range.

Drug Interactions

Prescriber should be aware of a number of iron/drug interactions, including antacids, tetracyclines, or fluoroquinolones.

Notice

Contact with moisture can discolor or erode the tablet. Do not chew tablet.

PRINCIPAL DISPLAY PANEL - 90 mg Tablet Bottle

NDC 13811-012-90
Rx Only

FerraPlus 90
Tablets
WITH 90 MG CARBONYL IRON

90 COATED TABLETS

TRIGEN
LABORATORIES

FerraPlus 90 
docusate sodium, folic acid, iron, cyanocobalamin, and ascorbic acid tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:13811-012
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Docusate Sodium (Docusate) Docusate Sodium 50 mg
Folic Acid (Folic Acid) Folic Acid 1 mg
Iron (Iron) Iron 90 mg
Cyanocobalamin (Cyanocobalamin) Cyanocobalamin 12 ug
Ascorbic acid (Ascorbic acid) Ascorbic acid 120 mg
Inactive Ingredients
Ingredient Name Strength
Cellulose, Microcrystalline  
Anhydrous Dibasic Calcium Phosphate  
Potassium Citrate Anhydrous  
Carboxymethylcellulose Sodium  
Acacia  
Povidone K30  
Croscarmellose Sodium  
Silicon Dioxide  
Stearic Acid  
Magnesium Stearate  
Citric Acid Monohydrate  
Icodextrin  
Dextrose  
Sodium Citrate  
Product Characteristics
Color GRAY (dark grey) Score no score
Shape OVAL Size 15mm
Flavor Imprint Code TL012
Contains     
Packaging
# Item Code Package Description
1 NDC:13811-012-90 90 TABLET, FILM COATED (TABLET) in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 09/01/2011
Labeler - TRIGEN Laboratories, Inc. (830479668)
Revised: 09/2011   TRIGEN Laboratories, Inc.
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