Caffeine Citrate Injection
Product Images NDC 0641-6267

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Caffeine Citrate (NDC 0641-6267). 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 Injection 1)

Chemical structure of caffeine citrate, showing the molecular arrangement of caffeine combined with citrate moiety as part of the structure.*

FDA Label Image

Ww Black Logo (Cafcit Injection 2)

Cafcit Injection 60 mg/3 mL (20 mg/mL) vial label for caffeine citrate injection USP, provided as a single-dose 3 mL vial for intravenous use. Label indicates it is prescription only and manufactured by West-Ward in Eatontown, NJ.*

FDA Label Image

Cafcit Injection Container Label 462-709-00 (Cafcit Injection 3)

Caffeine Citrate Injection, USP label for 60 mg/3 mL (20 mg/mL) solution in 10 single-dose vials. The label indicates it is for intravenous use only and single use, with the unused portion to be discarded. Manufactured by West-Ward in Eatontown, NJ, the label includes storage instructions at controlled room temperature (20° to 25°C). The label features the brand CAFCIT and specifies the drug is preservative free.*

FDA Label Image

Cafcit Injection Shelfpack Label 462-710-00 (Cafcit Injection 4)

The image shows a product label for Caffeine Citrate Injection 20 mg/mL by Hikma Pharmaceuticals USA Inc. The label includes a QR code, GTIN number 00301234567896, serial number 1234567890123, an expiration date format placeholder (MMYYYY), and a lot number placeholder (ABCDE12345). It is intended for intravenous use.*

* 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.