Marbeta 25 Kit
Product Images NDC 76420-785

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Marbeta 25 Kit (NDC 76420-785). 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

50caa3fb-figure-01 (Mar07 0004 01)

Chemical structure of Betamethasone Sodium Phosphate as part of the Marbeta 25 Kit active ingredients. The diagram shows a steroid backbone with phosphate and sodium groups attached, representing the molecular structure of this corticosteroid component.*

FDA Label Image

50caa3fb-figure-02 (Mar07 0004 02)

Chemical structure diagram of the active ingredient Betamethasone, showing its molecular framework and functional groups as part of the Marbeta 25 Kit components.*

FDA Label Image

Structural Formula Bupivacaine Hydrochloride (Mar07 0004 03)

Chemical structure of Bupivacaine Hydrochloride showing its molecular formula with piperidine ring, aromatic ring, and associated chloride and water molecules as represented in the image.*

FDA Label Image

Structural Formula Epinephrine (Mar07 0004 04)

Marbeta-25 Kit packaging label displays the product name prominently with the NDC 76420-785-01 and Rx Only indication. The label lists the kit contents: Bupivacaine HCl 0.25% single dose vial (10 mL), Betamethasone Sodium Phosphate and Betamethasone Acetate 6 mg/mL (5 mL), Povidone-Iodine swabsticks (3), Isopropyl Alcohol 70% prep pads (3), nitrile powder-free sterile gloves (pair, size M), one drape, adhesive bandage, and five non-sterile 4x4 gauze pads. Needles and syringes are not included. Distributed by Enovachem Pharmaceuticals, Torrance, CA.*

* 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.