Buprenorphine Hydrochloride Sublingual
Product Images NDC 67046-996

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hydrochloride Sublingual (NDC 67046-996). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Contract Pharmacy Services-pa, 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 Hydrochloride Sublingual Tablets Ciii 2 mg Bottle Label (D2288167 C532 4fb4 Abe3 F362492b9e5a 03)

Buprenorphine sublingual tablets are available in packs of 30. Each tablet contains 2.16 mg of Buprenorphine HCI which is equivalent to 2 mg of buprenorphine base. These tablets are classified as a controlled substance and should be stored at a temperature of 20-25°C. The CPS NDC for these tablets is 67046-996-30. The prescribing information is not available in the given text.*

FDA Label Image

Buprenorphine Hydrochloride Sublingual Tablets Ciii 8 mg Bottle Label (D2288167 C532 4fb4 Abe3 F362492b9e5a 04)

Buprenorphine Sublingual is a controlled medication available in the form of 8 mg tablets packed in a bottle of 30 tablets. The medication contains 8.84mg of buprenorphine HCl equivalent to 8 mg of buprenorphine base. It is prescribed in accordance with accompanying prescribing information. The lot number of the medication is TEST, and the pill ID is M 924. The medication is packaged by Contract Pharmacy Services in Pennsylvania. The storage recommendation for the medication is 20-25°C (88-77°F). The CPSNDC number of the medication is 67046-997-30.*

FDA Label Image

Buprenorphine Hydrochloride Structural Formula (Image 01)

FDA Label Image

Medication Guide Tablet Placement (Image 02)

* 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.