Phenobarbital Tablet
Product Images NDC 69367-626

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Phenobarbital (NDC 69367-626). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Westminster Pharmaceuticals, 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

Chemical Structure (Phenobarbital 01)

Chemical structure of phenobarbital. The diagram shows the molecular layout including a phenyl group, ethyl group, and three ketone groups attached to the pyrimidine ring.*

FDA Label Image

Principal Display Panel (16.2 mg Tablet Bottle Label)

Phenobarbital 16.2 mg (1/4 grain) tablets, USP label from Westminster Pharmaceuticals, LLC. The label states Rx Only, contains 100 tablets, includes a barcode, warning about habit forming, and storage instructions. The NDC is 69367-625-01.*

FDA Label Image

Principal Display Panel (32.4 mg Tablet Bottle Label)

Phenobarbital 32.4 mg (1/2 grain) tablets, USP, oral dosage form in a package label showing 100 tablets. Label includes the NDC 69367-626-01, indicates prescription only (Rx Only), and is manufactured by Westminster Pharmaceuticals, LLC.*

FDA Label Image

Principal Display Panel (64.8 mg Tablet Bottle Label)

Label for Phenobarbital tablets USP 64.8 mg (1 grain) by Westminster Pharmaceuticals, LLC. The label indicates the product contains 100 tablets, is prescription only, and includes warnings about habit formation and proper storage conditions. The UPC barcode and NDC number 69367-627-01 are also displayed.*

FDA Label Image

Principal Display Panel (97.2 mg Tablet Bottle Label)

Label for Phenobarbital tablets, USP 97.2 mg (1 1/2 grain) oral tablets by Westminster Pharmaceuticals, LLC. The label indicates 100 tablets per package, includes warnings about habit formation, storage instructions, and dosage guidelines. It also displays the NDC 69367-628-01 and a barcode.*

* 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.