Sumatriptan Injection, Solution
Product Images NDC 51407-673

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Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Sumatriptan (NDC 51407-673). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-673-01 (Sumatriptan Injector Label 6 mg0.5 mL)

51407-673-01 (Sumatriptan Injector Label 6 mg0.5 mL)
This text provides details about Sumatriptan Injection USP, a medication delivered through an autoinjector system for subcutaneous injections. Each autoinjector contains 0.5 mL of solution with 8.4 mg of sumatriptan succinate (equivalent to 6 mg of sumatriptan) and 3.5 mg of sodium chloride. The solution has a pH of approximately 4.2 to 5.3 and an osmolality of 270-330 mOsmol. It is sterile, nonpyrogenic, and should be stored between 2° and 30°C (36° and 86°F) while protected from light. This product is marketed by GSMS, Incorporated, in Camarillo, CA, USA, and is a product of Spain.*
FDA Label Image

51407-673-02 (Sumatriptan Injector Carton 6 mg0.5 mL)

51407-673-02 (Sumatriptan Injector Carton 6 mg0.5 mL)
This text contains instructions for using a disposable sumatriptan autoinjector system, including details on how to prepare and perform the injection. It provides step-by-step guidance on assembling the autoinjector, applying it to the skin, and monitoring the injection process through a medicine window. Additionally, the text includes essential information on the contents of the autoinjector, storage conditions, and warnings about not using the product if the tamper-evident seal is broken or missing.*
FDA Label Image

Sumatriptan-structure (7b0603f0 Ed39 460b 9d7b F19b95006024 01)

FDA Label Image

Device Image (7b0603f0 Ed39 460b 9d7b F19b95006024 02)

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Image Description (7b0603f0 Ed39 460b 9d7b F19b95006024 03)

Image Description (7b0603f0 Ed39 460b 9d7b F19b95006024 03)
This is a guide for using an autoinjector with a gray cap. It instructs users to remove the cap before the autoinjector will work. Additionally, it advises using a transparent window to check the liquid clarity and pressing the blue injection button firmly to start the injection.*
FDA Label Image

Figure A (7b0603f0 Ed39 460b 9d7b F19b95006024 04)

Figure A (7b0603f0 Ed39 460b 9d7b F19b95006024 04)
Not available.*
FDA Label Image

Figure B (7b0603f0 Ed39 460b 9d7b F19b95006024 05)

Figure B (7b0603f0 Ed39 460b 9d7b F19b95006024 05)
This is not-available.*
FDA Label Image

Figure C (7b0603f0 Ed39 460b 9d7b F19b95006024 06)

Figure C (7b0603f0 Ed39 460b 9d7b F19b95006024 06)
After Injection of medication, the Blue Plunger Rod fills the window on the device. This is shown in Figure C.*
FDA Label Image

Figure D (7b0603f0 Ed39 460b 9d7b F19b95006024 07)

FDA Label Image

Figure E (7b0603f0 Ed39 460b 9d7b F19b95006024 08)

FDA Label Image

Figure F (7b0603f0 Ed39 460b 9d7b F19b95006024 09)

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Figure G (7b0603f0 Ed39 460b 9d7b F19b95006024 10)

FDA Label Image

Figure H (7b0603f0 Ed39 460b 9d7b F19b95006024 11)

Figure H (7b0603f0 Ed39 460b 9d7b F19b95006024 11)
This is a description of an image showing a blue plunger moving down to fill medicine flow after injection.*
FDA Label Image

Figure I (7b0603f0 Ed39 460b 9d7b F19b95006024 12)

FDA Label Image

Figure J (7b0603f0 Ed39 460b 9d7b F19b95006024 13)

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Figure K (7b0603f0 Ed39 460b 9d7b F19b95006024 14)

FDA Label Image

Time To Relief Of Cluster Headache From Time Of Injectiona (7b0603f0 Ed39 460b 9d7b F19b95006024 17)

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