Duetact Tablet
Product Images NDC 64764-302

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Duetact (NDC 64764-302). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Takeda Pharmaceuticals America, 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

Duetact 01

Label for Duetact tablets containing pioglitazone 30 mg and glimepiride 2 mg. The label includes storage instructions, distributor information (Takeda Pharmaceuticals America, Inc.), and dosage form as oral tablets. It also features a barcode, NDC 64764-302-30, and a note to dispense with a medication guide available in the package insert or at the website www.duetact.com.*

FDA Label Image

Duetact 02

Duetact tablets blister pack label showing pioglitazone 30 mg and glimepiride 4 mg oral tablets. The label indicates the package contains 30 tablets from Takeda Pharmaceuticals America, Inc. Instructions for storage, dosage reference, and a medication guide notice are included, along with barcodes and the NDC 64764-304-30.*

FDA Label Image

Pio-chem Structure.jpg (F5942e7a F8c6 4b1a Be4f Ad47be5c954f 01)

Chemical structure of pioglitazone hydrochloride, an active ingredient in Duetact.*

FDA Label Image

Glim-chem Structure.jpg (F5942e7a F8c6 4b1a Be4f Ad47be5c954f 02)

Chemical structure diagram of glimepiride, one of the active ingredients in Duetact, showing its molecular composition with labeled chemical bonds and groups.*

* 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.