Miglitol
Product Images NDC 76333-125

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Miglitol (NDC 76333-125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Orient Pharma 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

Op 100mg 100s

Label for Miglitol tablets, 100 mg strength, containing 100 tablets. The label states each film-coated tablet contains 100 mg of miglitol. It includes storage instructions to keep at 25°C with permitted excursions to 15-30°C. The labeler is Orient Pharma Co., Ltd., based in Yunlin, Taiwan. The NDC number 76333-127-11 and Rx only status are visible.*

FDA Label Image

Op 25mg 100s

Miglitol Tablets 25 mg label for a package containing 100 film-coated tablets. The label includes storage instructions, states Rx only, and mentions Orient Pharma Co., Ltd. as the manufacturer in Yunlin, Taiwan. The NDC number 76333-125-11 is displayed along with a barcode.*

FDA Label Image

Op 50mg 100s

Miglitol 50 mg tablets packaging label by Orient Pharma Co., Ltd. The label states 100 film-coated tablets per bottle, includes storage instructions at 25°C (77°F) with permitted excursions, and displays the NDC code 76333-126-11. The manufacturer is located in Yunlin, Taiwan.*

FDA Label Image

Chemical Structure (Miglitol 01)

Chemical structure of the active ingredient Miglitol as depicted in a molecular diagram showing its compound arrangement and functional groups.*

FDA Label Image

Figures (Miglitol 02)

Two bar graphs showing the mean change from baseline treatment effect of Miglitol at doses of 25 mg, 50 mg, and 100 mg taken three times daily (tid). Figure 1 depicts the mean change in HbA1c (%) with dose-dependent decreases, and Figure 2 shows the mean change in 1-hour postprandial plasma glucose (mg/dL), both presenting pooled results from controlled fixed-dose studies.*

FDA Label Image

Principal Display Panel (25 mg Tablet Bottle Label)

Label for Miglitol Tablets, 25 mg, with a package count of 1,000 tablets. The label includes storage instructions, dosage direction to see prescribing information, and manufacturing details by Orient Pharma Co., Ltd. in Yunlin, Taiwan. It also displays the NDC number 76333-125-12, a barcode, and branding for Orient Pharma.*

FDA Label Image

Principal Display Panel (50 mg Tablet Bottle Label)

Miglitol Tablets 50 mg label from Orient Pharma Co., Ltd. The label indicates a package of 1,000 tablets with prescription-only status. Storage instructions specify 25°C (77°F) with permitted excursions to 15-30°C. The label includes a barcode, NDC number 76333-126-12, and manufacturing location in Yunlin, Taiwan.*

FDA Label Image

Principal Display Panel (100 mg Tablet Bottle Label)

Label for Miglitol Tablets 100 mg, containing 1,000 film-coated tablets. The label shows storage instructions at 25°C with permitted excursions, states each tablet contains 100 mg of miglitol, and includes references to prescribing information. Manufactured by Orient Pharma Co., Ltd, Taiwan. The label includes an NDC barcode and space for lot and expiration dates.*

* 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.