Buprenorphine Hydrochloride Injection
Product Images NDC 68083-696

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hydrochloride (NDC 68083-696). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma 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

Buprenorphine-spl-structure (Buprenorphine Spl Structure)

Chemical structure of Buprenorphine hydrochloride, illustrating its molecular framework including multiple rings and functional groups characteristic to this active ingredient.*

FDA Label Image

Buprenorphine-spl-vial-label (Buprenorphine Spl Vial Label)

Label for Buprenorphine Hydrochloride Injection 0.3 mg/mL in a 1 mL single-dose vial. Intended for intramuscular or intravenous use, the label shows the active ingredient strength as 0.324 mg per mL of buprenorphine HCl, equivalent to 0.3 mg buprenorphine. Manufactured by Gland Pharma Limited, with storage instructions to protect from light and a note to discard unused portion. The label includes a barcode and space for lot and expiration information.*

FDA Label Image

Buprenorphine-spl-carton-label (Buprenorphine Spl Carton Label)

Packaging label for Buprenorphine Hydrochloride Injection 0.3 mg/mL, an intramuscular and intravenous injection presented in 5 x 1 mL single-dose vials. Labeler is Gland Pharma Limited. The label includes dosage instructions, storage conditions, and barcode, marked Rx Only with a controlled substance symbol (III).*

* 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.