Acarbose Tablet
Product Images NDC 71335-9725

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acarbose (NDC 71335-9725). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Structure (B19003ee Dd84 4104 Bcbc Ce752962aa59 01)

Structure (B19003ee Dd84 4104 Bcbc Ce752962aa59 01)
Chemical structure diagram of acarbose showing its molecular arrangement. The structure illustrates multiple sugar-like rings connected by oxygen atoms, hydroxyl groups (OH), and other bonds characteristic of the acarbose molecule.*
FDA Label Image

Figure 1 (B19003ee Dd84 4104 Bcbc Ce752962aa59 02)

Figure 1 (B19003ee Dd84 4104 Bcbc Ce752962aa59 02)
Bar chart titled 'Dose of Acarbose tablets (t.i.d)' showing mean change in plasma glucose (mg/dL) for doses 25 mg, 50 mg, 100 mg, 200 mg, and 300 mg. Each bar includes the sample size (N) for each dose group. The y-axis ranges from 0 to -100 mg/dL indicating a decrease in plasma glucose values.*
FDA Label Image

Figure2 (B19003ee Dd84 4104 Bcbc Ce752962aa59 03)

Figure2 (B19003ee Dd84 4104 Bcbc Ce752962aa59 03)
A figure labeled 'Figure 2' showing four line graphs labeled A to D for Diet, Sulfonylurea, Metformin, and Insulin, respectively. Each graph plots variables over 0 to 12 months on the x-axis against a numerical scale from -1.5 to 1.5 on the y-axis, illustrating changes in measurements for different treatments across time intervals.*
FDA Label Image

Label (Lbl713359725)

Label (Lbl713359725)
Acarbose Tablets USP 50 mg oral tablets packaged in a container holding 30 tablets. The label includes storage instructions, safety warnings, and is marked Rx only. It is repackaged by Bryant Ranch Prepack, Inc. in Burbank, California, and manufactured by RA Chem Pharma Limited. The NDC code is 71335-9725-1.*

* 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.