Epinephrine Injection
Product Images NDC 76420-834

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Epinephrine (NDC 76420-834). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed 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 (Epinephrine Injection 1)

Chemical Structure (Epinephrine Injection 1)
Chemical structure diagram depicting the molecular formula of epinephrine, showing its characteristic catechol ring with hydroxyl groups and side chain containing an amine group.*
FDA Label Image

1 (Epinephrine Injection 2)

1 (Epinephrine Injection 2)
An illustration labeling parts of an epinephrine auto-injector and its carrying case. The auto-injector is shown with a red tip for the needle end, a viewing window, labeled dosage (0.15 mg), and blue end caps. The carrying case is shown separately, in orange with ridges for grip.*
FDA Label Image

1 (Epinephrine Injection 3)

1 (Epinephrine Injection 3)
Illustration of an epinephrine auto-injector 0.3 mg showing components labeled: carrying case, end caps, needle end with red tip, viewing window, and auto-injector body.*
FDA Label Image

Figure A (Epinephrine Injection 4)

Figure A (Epinephrine Injection 4)
An instructional diagram illustrating the first step for using an epinephrine subcutaneous injection. The image shows the syringe with two blue caps on both ends labeled to indicate they should be pulled off. Text and arrows emphasize pulling off both blue caps prior to injection.*
FDA Label Image

Figure B (Epinephrine Injection 5)

Figure B (Epinephrine Injection 5)
Instructional illustration labeled Figure B showing how to use an epinephrine subcutaneous injection. It depicts a hand holding the injector with the red tip pressed against the thigh, indicating to push the red tip hard into the thigh for 10 seconds.*
FDA Label Image

Figure C (Epinephrine Injection 6)

Figure C (Epinephrine Injection 6)
An instructional illustration labeled Figure C showing two hands preparing a subcutaneous injection. One hand holds a syringe containing red liquid, and the other hand is removing the cap from the needle with an arrow indicating the direction to pull the cap off.*
FDA Label Image

Figure D (Epinephrine Injection 7)

Figure D (Epinephrine Injection 7)
An instructional diagram labeled Figure D showing two hands holding a syringe with a label marked "epinephrine". An arrow indicates the syringe is being pushed or advanced over a surface, depicting part of the preparation or administration process for epinephrine injection.*
FDA Label Image

1 (Epinephrine Injection 8)

1 (Epinephrine Injection 8)
This image shows two label panels for epinephrine injection USP auto-injector 0.3 mg, relabeled by Enovachem Pharmaceuticals. Each label includes NDC numbers 76420-834-01 and 76420-834-02 with quantities of 1 and 2 auto-injectors respectively. The labels state the product is a single-dose, pre-filled auto-injector distributed by Amneal Pharmaceuticals LLC, with storage instructions and federal law cautions.*
FDA Label Image

1 (Epinephrine Injection 9)

1 (Epinephrine Injection 9)
This image shows labeling for epinephrine injection USP auto-injectors at a strength of 0.15 mg. The labels indicate two products with NDC codes 76420-835-01 and 76420-835-02, distributed by Amneal Pharmaceuticals LLC, relabeled by Enovachem Pharmaceuticals in Torrance, CA. Each label includes quantity, lot, batch, and caution statements regarding prescription status and storage instructions.*

* 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.