Buprenorphine And Naloxone Film, Soluble
Product Images NDC 43598-581

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Buprenorphine And Naloxone (NDC 43598-581). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddys Laboratories 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

Carton1 (Carton1)

Carton1 (Carton1)
This is a combination drug product containing buprenorphine and naloxone, used to treat addiction to opioids. It is dispensed as a sublingual film (a film placed under the tongue) and is only available by prescription. The packaging includes a warning to keep the product out of the reach of children, as accidental exposure can be dangerous. The exact quantity of the product is not clear, but it appears to be 50 pouches containing the sublingual films and made by Dr. Reddy's.*
FDA Label Image

Carton2 (Carton2)

FDA Label Image

Figure1 (Figure1)

FDA Label Image

Figure2 (Figure2)

FDA Label Image

Figure3 (Figure3)

FDA Label Image

Figure4 (Figure4)

FDA Label Image

Pouch1 (Pouch1)

Pouch1 (Pouch1)
Description: This appears to be a label of a medicine called "Sozma VS" by Dr. Reddys. The medicine comes in a sublingual film form with a strength of 4 mg/1mg. The text also mentions the NDC code of the medicine as 43598-580-01. The remaining text seems to be a mix of random symbols and characters, and hence, not available for making sense of.*
FDA Label Image

Pouch2 (Pouch2)

Pouch2 (Pouch2)
This appears to be a product description for a medication named "Buprenorphine" produced by a company named "Dr. Reddys". The medication is administered sublingually (under the tongue) and contains a combination of 12mg/3mg of the active ingredient. The NDC (National Drug Code) for the medication is 43598-581:01. The remaining characters are not readable.*
FDA Label Image

Structure1 (Structure1)

FDA Label Image

Structure2 (Structure2)

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