Vitrexate

Vitrexate is an FDA drug label for the active ingredient FOLIC ACID manufactured by PureTek Corporation administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230111.

Generic: FOLIC ACID

Manufacturer: PureTek Corporation

Product Type: HUMAN PRESCRIPTION DRUG

Route: ORAL

Dosage Form:

NDC: 59088-167

Application:

Effective: 20230111

Indications & Usage

INDICATIONS: To provide vitamin supplements to men and women. Folic acid is effective in the treatment of megaloblastic anemias due to a deficiency of folic acid (as may be seen in tropical or nontropical sprue) and in anemias of nutritional origin, pregnancy, infancy, or childhood.

Dosage & Administration

DOSAGE AND ADMINISTRATION: One (1) caplet daily, between meals or as directed by a physician. Do not administer to children under the age of 12.

Contraindications

CONTRAINDICATIONS: Contraindicated in patients with a known hypersensitivity to any of the ingredients.

Warnings

WARNING: Administration of folic acid alone is improper therapy for pernicious anemia and other megaloblastic anemias in which vitamin B12 is deficient.

Adverse Reactions

Adverse Reactions: Allergic sensitization has been reported following both oral and parenteral administration of folic acid. Adverse reactions have been reported with specific vitamins and minerals but generally at levels substantially higher than those contained herein. However, allergic and idiosyncratic reactions are possible at lower levels. Iron, even at the usually recommended levels, has been associated with gastrointestinal intolerance in some patients.

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