Vykoura Injection
Product Images NDC 83831-148

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Vykoura (NDC 83831-148). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avyxa Pharma, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Image (035ed9b1 F54a 4191 B999 845cdb4540fc 01)

Chemical structure of leucovorin calcium, the active ingredient in VYKOURA injection, depicting the molecular arrangement of atoms including calcium ion and associated organic groups.*

FDA Label Image

Vykoura (leucovorin) Injection, 50 mg/5 mL -container Label (035ed9b1 F54a 4191 B999 845cdb4540fc 02)

VYKOURA (leucovorin calcium) Injection label for 50 mg per 5 mL (10 mg per mL) strength. The label states it is for intravenous or intramuscular use. It includes content information per mL, storage instructions, manufacturer Avyxa Pharma, LLC, and lot and expiration date fields. The vial is single-dose with unused portion to be discarded.*

FDA Label Image

Vykoura (leucovorin) Injection, 50 mg/5 mL -carton Label (035ed9b1 F54a 4191 B999 845cdb4540fc 03)

VYKOURA (leucovorin calcium) Injection label for 50 mg per 5 mL (10 mg per mL) dosage form. The label indicates use for intravenous or intramuscular injection and mentions a single-dose 5 mL vial. It includes storage instructions to keep refrigerated and states the product is manufactured for Avyxa Pharma, LLC. The label also includes the NDC 83831-147-05 and barcode.*

FDA Label Image

Vykoura (leucovorin) Injection, 350 mg/35 mL -container Label (035ed9b1 F54a 4191 B999 845cdb4540fc 04)

VYKOURA (leucovorin calcium) Injection label for 350 mg per 35 mL (10 mg per mL), intended for intravenous or intramuscular use. The label indicates one single-dose vial with instructions to discard any unused portion. The label includes storage instructions, active ingredient details, manufacturer Avyxa Pharma, LLC, and barcodes.*

FDA Label Image

Vykoura (leucovorin) Injection, 350 mg/35 mL -carton Label (035ed9b1 F54a 4191 B999 845cdb4540fc 05)

Packaging label for VYKOURA (leucovorin calcium) Injection 350 mg per 35 mL (10 mg per mL) by Avyxa Pharma, LLC. The label indicates it is for intravenous or intramuscular use, comes in a single-dose 35 mL vial, and includes storage instructions to keep refrigerated between 2°C to 8°C. The label specifies this is a prescription-only drug and notes the container closure is not made with natural rubber latex.*

FDA Label Image

Vykoura (leucovorin) Injection, 500 mg/50 mL -conatiner Label (035ed9b1 F54a 4191 B999 845cdb4540fc 06)

VYKOURA (leucovorin calcium) Injection label showing 500 mg per 50 mL (10 mg per mL) strength. It indicates use for intravenous or intramuscular administration with one single-dose vial and discard unused portion instructions. Manufactured by Avyxa Pharma, LLC, Newark, New Jersey. Label includes ingredients, storage, and dosage information alongside a barcode and NDC 83831-149-50.*

FDA Label Image

Vykoura (leucovorin) Injection, 500 mg/50 mL -carton Label (035ed9b1 F54a 4191 B999 845cdb4540fc 07)

Packaging label for VYKOURA (leucovorin calcium) Injection 500 mg per 50 mL (10 mg/mL) from Avyxa Pharma, LLC. The label specifies the product is for intravenous or intramuscular use, containing one 50 mL single-dose vial. Storage instructions advise refrigeration at 2°C to 8°C and protection from light. The label includes barcodes and manufacturing information indicating it is made in Switzerland.*

FDA Label Image

Image (254d9fbe 583c 4463 9f0f E640764def0c 120 1)

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.