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NataFort

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Generic:Ascorbic acid, Cholecalciferol, .alpha.-tocopherol acetate, dl-, Thiamine mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, and Iron
Manufacturer:Mission Pharmacal Company
Drug Classes:Not Available
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NataFort

Generic:Ascorbic acid, Cholecalciferol, .alpha.-tocopherol acetate, dl-, Thiamine mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, and Iron
Manufacturer:Mission Pharmacal Company
Drug Classes:Not Available
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Synopsis
Contents
Black Box WarningDescriptionIndication and UsageHow suppliedDosage & Side EffectsContraindicationsWarningsAdverse Reactions
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Synopsis
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Disclaimer: The synopsis and product information provided on Alpha.MD are derived from openFDA data and are for informational purposes only. This information may not be comprehensive, accurate, or up-to-date. Clinicians should exercise their own professional judgment in interpreting and using this information, and consult the official prescribing information for the most accurate and current details.
Black Box Warning

WARNING Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. In case of accidental overdose, call a doctor or poison control center immediately.

Description

DESCRIPTION NataFort ® is a prescription prenatal/postnatal multivitamin/mineral supplement. The tablet is white, coated, and oval in shape, and is debossed "N1" on one side and is blank on the other. Each prenatal tablet contains: Vitamin C (Ascorbic acid) 120 mg Vitamin D 3 (Cholecalciferol) 400 IU Vitamin E (dl-alpha tocoperyl acetate) 11 IU Thiamin (Vitamin B 1 ) 2 mg Riboflavin (Vitamin B 2 ) 3 mg Niacinamide (Vitamin B 3 ) 20 mg Vitamin B 6 (Pyridoxine HCl) 10 mg Folic Acid 1 mg Vitamin B 12 (Cyanocobalamin) 12 mcg Iron (Ferrous fumarate, carbonyl iron) 60 mg

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Indication and Usage

INDICATIONS NataFort ® is a multivitamin/mineral prescription drug indicated for use in improving the nutritional status of women prior to conception, throughout pregnancy, and in the postnatal period for both lactating and nonlactating mothers.

How supplied

HOW SUPPLIED Bottles of 90 tablets each - NDC 0178-0716-90.

Dosage & Side Effects

DOSAGE AND ADMINISTRATION One tablet daily or as directed by a physician.

Contraindications

CONTRAINDICATIONS This product is contraindicated in patients with a known hypersensitivity to any of the ingredients.

Warnings

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

Adverse Reactions

ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

Approval History
FDA approved 2011
Includes history for all formulations of adalimumab
August 10, 2011
(Type 2 New Active Ingredient and Type 4 New Combination)
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