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Prescription products · Product label record

Vitavera drug information

VITAVERA
Oncora Pharma, LLC · ORAL

Product NDC: 85477-513

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameVITAVERA
Labeler / manufacturerOncora Pharma, LLC
RouteORAL
Drug classVitamin A / Vitamin C / Nicotinic Acid / Vitamin B6 Analog / Folate Analog
Product NDC85477-513
Label effective date2026-04-21

Official product label reference

Vitavera — Oncora Pharma, LLC

This page contains 14 source sections for VITAVERA, oral route. Label set 058b1921-21da-49d9-b9c1-3f5636087aea, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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 and administration — label text
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.
Drug interactions
Drug Interactions
Product description
DESCRIPTION Vitavera™ is a chewable multivitamin dietary supplement containing essential vitamins including Vitamins A, C, D, E, B-complex vitamins, and folate. It is formulated to support general nutritional supplementation and overall health.
Precautions
PRECAUTIONS Folic acid in doses above 0.1 mg daily may obscure pernicious anemia, in that hematologic remission can occur while neurological manifestations remain progressive. The patient’s medical condition and concurrent use of medications, herbs, or supplements should be considered prior to use. If pregnant, lactating, or trying to conceive, consult a licensed healthcare professional prior to use. General Drug Interactions Carcinogenesis, Mutagenesis, Impairment of Fertility Pregnancy Nursing Mothers Pediatric Use
General precautions
General
Carcinogenesis and mutagenesis and impairment of fertility
Carcinogenesis, Mutagenesis, Impairment of Fertility
Pregnancy
Pregnancy
Breastfeeding
Nursing Mothers
Children and adolescents
Pediatric Use
Overdose information
OVERDOSAGE In case of accidental overdose, seek professional assistance or contact a poison control center immediately.
Supply and packaging
HOW SUPPLIED Vitavera™ chewable multivitamin tablets are supplied as: 30 tablets per bottle NDC: 85477-513-30 Round chewable tablets, cherry flavored Dispense in a tight, light-resistant container as defined in the USP.

Official sources and product identifiers

Substances listed: VITAMIN A, ASCORBIC ACID, SODIUM ASCORBATE, VITAMIN D, ALPHA-TOCOPHEROL ACETATE, THIAMINE, RIBOFLAVIN, NIACIN, PYRIDOXINE, LEVOMEFOLIC ACID, METHYLCOBALAMIN

Package NDC codes

85477-513-30

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.