Bupivacaine Hydrochloride Injection
Product Images NDC 73293-0002

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Bupivacaine Hydrochloride (NDC 73293-0002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Huons Co., Ltd., 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

Ampule Label (Ampule Label 2ml)

Label for Bupivacaine Hydrochloride 7.5 mg/mL injection, USP in a 2 mL ampule for subarachnoid (spinal) administration. The label shows active ingredient concentrations of 0.75% bupivacaine HCl and 8.25% dextrose, includes an NDC number 73293-0002-1, barcode, lot number, and expiration date space. Manufactured by Huons Co., Ltd.*

FDA Label Image

Bupivacaine Formula (Bupivacaine Formula)

Chemical structure of Bupivacaine hydrochloride showing its molecular components including a piperidine ring, aromatic ring with methyl groups, amide linkage, and associated hydrochloride and water molecules.*

FDA Label Image

Carton Label (Carton Label 50ampoules 10)

Packaging label for Bupivacaine Hydrochloride in Dextrose Injection, USP, 0.75% (Bupivacaine HCl) and 8.25% (Dextrose) strength, sterile hyperbaric solution for spinal anesthesia. The label indicates 50 single-dose 2 mL ampules. Manufactured by Huons Co., Ltd., Korea. The label shows product name, strength, dosage form, route (spinal), and storage instructions.*

FDA Label Image

Dextrose Formula (Dextrose Formula 1)

Chemical structure diagram showing the molecular structure of Bupivacaine hydrochloride with a water molecule (H2O) indicated, consistent with the product Bupivacaine Hydrochloride injection by Huons Co., Ltd.*

* 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.