Metronidazole Tablet
Product Images NDC 65862-694

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metronidazole (NDC 65862-694). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (250 mg (50 Tablets Bottle))

Label for Metronidazole Tablets USP 250 mg oral tablets by Aurobindo Pharma Limited. The label shows a 50 tablet count, includes storage instructions, dosage caution, and distributor information for Aurobindo Pharma USA, Inc. Made in India with barcode and coding area noted.*

FDA Label Image

Package Label-principal Display Panel (500 mg (50 Tablets Bottle))

Label for Metronidazole 500 mg oral tablets, containing 50 tablets per container. The label states it is for prescription use (Rx only) and provides storage instructions at 20° to 25°C. Distributed by Aurobindo Pharma USA, Inc., made in India. Includes NDC 65862-695-50, barcode, and instructions to protect from light and dispense in child-resistant containers.*

FDA Label Image

Chemical Structure (Metronidazole Str)

Chemical structure diagram of Metronidazole showing the molecular arrangement including a nitro group, an imidazole ring, and an ethanol side chain.*

FDA Label Image

Symbol (Metronidazole Symbol)

Metronidazole 500 mg oral tablet packaging label from Aurobindo Pharma Limited. The label prominently displays the brand name Metronidazole and dosage strength 500 mg. It includes the active ingredient name and quantity per tablet, along with manufacturer details. The label background is primarily white with blue and red accent colors.*

* 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.