Sumatriptan Injection
Product Images NDC 0143-9638

6 FDA label images from Hikma Pharmaceuticals Usa Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Sumatriptan (NDC 0143-9638). 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

Chemical Structure (Sumatriptan Injection Usp 1)

Chemical Structure (Sumatriptan Injection Usp 1)
Chemical structure of sumatriptan, the active ingredient in SUMATRIPTAN injection. The diagram shows the molecular arrangement including a substituted indole structure and functional groups characteristic of sumatriptan.*
FDA Label Image

Figure 1. Time To Relief Of Cluster Headache From Time Of Injection (Sumatriptan Injection Usp 2)

Figure 1. Time To Relief Of Cluster Headache From Time Of Injection (Sumatriptan Injection Usp 2)
A line graph showing the estimated percentage of subjects with relief over time in minutes, comparing Sumatriptan injection (N=131) and placebo (N=127). The graph indicates higher relief percentages for Sumatriptan compared to placebo throughout the 25-minute duration.*
FDA Label Image

Ndc 0143-9638-01 Sumatriptan Injection, Usp 6 mg (base)/0.5 mL For Subcutaneous Injection Only Rx Only 0.5 mL Single Dose Vial Store Between 2º And 30ºc (36º To 86ºf). Protect From Light. (Sumatriptan Injection Usp 3)

Ndc 0143-9638-01 Sumatriptan Injection, Usp 6 mg (base)/0.5 mL For Subcutaneous Injection Only Rx Only 0.5 mL Single Dose Vial Store Between 2º And 30ºc (36º To 86ºf). Protect From Light. (Sumatriptan Injection Usp 3)
Label for SUMATRIPTAN injection, USP 6 mg/0.5 mL by Hikma Pharmaceuticals USA Inc. It indicates a 0.5 mL single dose vial for subcutaneous injection only. The label includes dosage strength, route, a barcode, and placeholders for lot number and expiration date.*
FDA Label Image

Ndc 0143-9638-05 5 X 0.5 mL Single Dose Vials Sumatriptan Injection, Usp 6 mg/0.5 mL For Subcutaneous Injection Only Rx Only (Sumatriptan Injection Usp 4)

Ndc 0143-9638-05 5 X 0.5 mL Single Dose Vials Sumatriptan Injection, Usp 6 mg/0.5 mL For Subcutaneous Injection Only Rx Only (Sumatriptan Injection Usp 4)
Packaging label for SUMATRIPTAN 6 mg/0.5 mL injection, USP, subcutaneous route. The label indicates 5 single-dose vials of 0.5 mL each. It is a human prescription drug by Hikma Pharmaceuticals USA Inc. The label includes dosage strength, administration route, and a note for Rx only.*
FDA Label Image

25 X 0.5 mL Single Dose Vials Ndc 0143-9638-25 Sumatriptan Injection, Usp 6 mg/0.5 mL For Subcutaneous Injection Only Rx Only (Sumatriptan Injection Usp 5)

25 X 0.5 mL Single Dose Vials Ndc 0143-9638-25 Sumatriptan Injection, Usp 6 mg/0.5 mL For Subcutaneous Injection Only Rx Only (Sumatriptan Injection Usp 5)
Packaging label for SUMATRIPTAN Injection USP 6 mg/0.5 mL by Hikma Pharmaceuticals USA Inc. The label indicates the product is a subcutaneous injection with a single-dose vial. The label includes the product NDC 0143-9638 and dosing strength, with instructions for storage and usage, and branding for West-Ward Pharmaceuticals.*
FDA Label Image

Sumatriptan Injection Usp 6

Sumatriptan Injection Usp 6
Label panel displaying a QR code and text fields for GTIN, serial number (SN), expiration date (EXP), and lot number (LOT). The GTIN is shown as 00301234567896, with example placeholders for the SN, EXP, and LOT. No specific product name or dosage information is visible in the image.*

* 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.