Sumatriptan Injection, Solution
Product Images NDC 65145-118

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sumatriptan (NDC 65145-118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Caplin Steriles Limited, 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 04 (Sumatriptan Carton)

Image 04 (Sumatriptan Carton)
This product is a Sumatriptan Injection for subcutaneous injection only. The package includes 5 single-dose vials of 0.5mL each. The unvarnished area on the package can be used for batch overprinting, including 2D code, Sr. No, GTIN, Lot number, and Exp date details which will be printed during online packing. The product must be discarded unused and stored between 20-30°C. This product is for Rx only and the manufacturer is Cap s Limited.*
FDA Label Image

Sumatriptan-image01 (Sumatriptan Image01)

FDA Label Image

Image2 (Sumatriptan Image02)

Image2 (Sumatriptan Image02)
This is a clinical trial result comparing the effectiveness of placebo versus Sumatriptan in terms of estimating the percentage of patients experiencing relief. The numbers are as follows: among 127 patients receiving placebo, the estimated percentage of patients experiencing relief is 100%, and among 131 patients receiving Sumatriptan, the estimated percentage of patients experiencing relief is not given. The time frame of the trial was 25 minutes.*
FDA Label Image

Sumatriptan-vial-6mg (Sumatriptan Vial 6mg)

Sumatriptan-vial-6mg (Sumatriptan Vial 6mg)
Sumatriptan Injection is a medicine manufactured by Caplin Steriles Limited in India. It is available in a 0.5 mL single-dose vial for subcutaneous injection only. The lot number and expiry date are provided. The text also includes instructions to protect the medication from light and to discard any unused portion. The drug is for prescription use only with the NDC code 65145-118-01. The remaining text is not legible.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.