Folyra

Folyra is an FDA-registered drug product whose active ingredient is MULTIVITAMIN. It is labelled by Oncora Pharma, LLC taken by oral and marketed as a human prescription drug product. Identifiers on file: NDC 85477-523, label effective 20260428. It is one of 6 FDA drug label records sharing the active ingredient MULTIVITAMIN. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing MULTIVITAMIN are most often described in connection with: usage folyra, prescription multivitamin, multimineral dietary, supplement indicated, management patients, suboptimal nutritional, status requiring, supplementation folate. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

INDICATIONS AND USAGE Folyra is a prescription multivitamin/multimineral dietary supplement indicated for the clinical dietary management of patients with suboptimal nutritional status requiring supplementation of folate and B vitamins, under physician supervision.

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

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

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

ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folic acid. Call your doctor for medical advice about adverse reactions. To report suspected adverse reactions or obtain product information, contact Oncora Pharma at 888-321-2821.

FDA lists 6 drug label records with MULTIVITAMIN as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Folyra used for?
INDICATIONS AND USAGE Folyra is a prescription multivitamin/multimineral dietary supplement indicated for the clinical dietary management of patients with suboptimal nutritional status requiring supplementation of folate and B vitamins, under physician supervision.

Who makes Folyra?
Oncora Pharma, LLC is the labeler of record for Folyra. 6 FDA label records share the active ingredient MULTIVITAMIN, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Folyra come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Folyra prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing MULTIVITAMIN?
Yes. 6 FDA drug label records list MULTIVITAMIN as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Folyra been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.