Glipizide Tablet, Extended Release
Product Images NDC 16714-894

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Glipizide (NDC 16714-894). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc., 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

Glipezide Usp (26f0c341 A482 4dc1 Aaef F0a92a84937c 01)

Chemical structure diagram of Glipizide, showing its molecular connectivity with characteristic rings and functional groups.*

FDA Label Image

2.5 mg (26f0c341 A482 4dc1 Aaef F0a92a84937c 02)

Glipizide Extended-release Tablets USP 2.5 mg oral tablet label for a package containing 30 tablets. The label includes dosage strength, quantity, manufacturer Northstar Rx LLC, and specifies packaging storage and handling instructions. The label also mentions the use of FD&C Yellow No. 5 as a color additive and the product's origin from India.*

FDA Label Image

5 mg (26f0c341 A482 4dc1 Aaef F0a92a84937c 03)

Label for Glipizide Extended-release Tablets, USP, 5 mg strength. The label indicates it is a prescription oral tablet product containing 100 tablets. It includes storage instructions, child-resistant packaging information, and manufacturer details: Northstar Rx LLC and Zydus Lifesciences Ltd. Barcode and NDC number 16714-895-01 are visible.*

FDA Label Image

10 mg (26f0c341 A482 4dc1 Aaef F0a92a84937c 04)

Glipizide Extended-release Tablets USP 10 mg, oral tablet packaging label. The label shows a 100-tablet package manufactured for Northstar Rx LLC and produced by Zydus Lifesciences Ltd. in India. It includes storage instructions, child-resistant package indication, and dosage reference to the package insert.*

* 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.