Cafcit
Product Images NDC 0641-6164

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cafcit (NDC 0641-6164). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., 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

Structural Formula (Cafcit Caffeine Citrate Injection 1)

Chemical structure of caffeine citrate showing the molecular arrangement of caffeine combined with citrate, including methylated nitrogen atoms and carboxyl groups.*

FDA Label Image

Unit Label (Cafcit Caffeine Citrate Injection 2)

Cafcit Injection, caffeine citrate injection USP, 60 mg per mL (20 mg per mL caffeine citrate), in a 3 mL single-dose vial. Label indicates single-use only and discard unused portion. Manufactured by West-Ward, Taunton, MA, marketed by Hikma Pharmaceuticals USA Inc. Storage instructions are included.*

FDA Label Image

Carton Label (Cafcit Caffeine Citrate Injection 3)

Label for Caffeine Citrate Injection (caffeine citrate injection, USP) 60 mg/3 mL (20 mg/mL) by Hikma Pharmaceuticals USA Inc. The label indicates the product is for intravenous use only and comes in 10 single-dose vials of 3 mL each. It includes storage instructions, prescribing restrictions, and manufacturer information from West-Ward in Eatontown, NJ.*

FDA Label Image

Layout 1 (Cafcit Caffeine Citrate Injection 4)

Label panel displaying a QR code and human-readable information including GTIN, serial number (SN), expiration date (EXP), and lot number (LOT) fields. The text includes placeholders for these values. The label is presumably for Caffeine Citrate by Hikma Pharmaceuticals USA Inc., product NDC 0641-6164.*

* 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.