Vitavera
Vitavera is an FDA drug label for the active ingredient VITAVERA manufactured by Oncora Pharma, LLC 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 20260421.
- Generic name
- VITAVERA
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 85477-513
- Application
- N/A
- Label effective
- 20260421
About this product
Vitavera is an FDA-registered drug product whose active ingredient is VITAVERA. It is labelled by Oncora Pharma, LLC taken by oral and marketed as a human prescription drug product. Identifiers on file: NDC 85477-513, label effective 20260421. 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.
What it is used for
Across FDA labelling, products containing VITAVERA are most often described in connection with: usage vitavera, indicated provide, supplemental amounts, essential vitamins, thiamine riboflavin, niacin vitamin, folate intended, help prevent. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
INDICATIONS AND USAGE Vitavera™ is indicated to provide supplemental amounts of essential vitamins including Vitamins A, C, D, E, thiamine, riboflavin, niacin, vitamin B6, vitamin B12, and folate. It is intended to supplement the diet and help prevent nutritional deficiencies. Formulated for use in patients requiring vitamin supplementation as directed by a licensed healthcare practitioner.
Dosage & Administration
DOSAGE AND ADMINISTRATION Usual adult dosage is one tablet daily , to be dissolved in the mouth or chewed before swallowing , or as directed by a licensed healthcare practitioner
Warnings
WARNINGS 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
ADVERSE REACTIONS Allergic sensitization has been reported following oral administration of folic acid. Adverse reactions are generally rare at recommended dosages; however, hypersensitivity reactions may occur.
Frequently asked questions
What is Vitavera used for?
INDICATIONS AND USAGE Vitavera™ is indicated to provide supplemental amounts of essential vitamins including Vitamins A, C, D, E, thiamine, riboflavin, niacin, vitamin B6, vitamin B12, and folate. It is intended to supplement the diet and help prevent nutritional deficiencies. Formulated for use in patients requiring vitamin supplementation as directed by a licensed healthcare practitioner.
Who makes Vitavera?
Oncora Pharma, LLC is the labeler of record for Vitavera.
What form does Vitavera 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 Vitavera 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.
Has Vitavera 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.