Metronidazole Tablet
Product Images NDC 67296-0078

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Metronidazole (NDC 67296-0078). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Metronidazole (20220818125210 00001)

This is a description of Metronidazole 500mg tablets, indicated for adults only. Each package contains 30 tablets with a lot number and expiration date for quality control. Instructions for dosage and storage conditions are provided. The manufacturer is Teva Czech Industries located in Czech Republic, and the distributor is Redpharm Drug in Eden Prairie, MN.*

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Structural Formula (Image 1)

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Chemical Equation Symbol (Image 2)

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1 (Image 3)

This is a description of Metronidazole 250 mg Tablets USP. Each tablet contains 250 mg of Metronidazole. The usual dosage instructions can be found in the package insert. It should be stored at 20° to 25°C (68° to 77°F) and protected from light. The medication should be kept out of reach of children. The tablets are manufactured in the Czech Republic by Teva Czech Industries and distributed by Teva Pharmaceuticals USA, Inc. The NDC number for the product is 50111-333-01 and the package contains 100 tablets.*

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2 (Image 4)

This is a packaging label for Metronidazole Tablets USP, with each tablet containing 500 mg of metronidazole. The recommended storage condition is between 20°C to 25°C (68°F to 77°F), and it needs protection from light. The medication should be kept in a tight, light-resistant container with a child-resistant closure. The manufacturer is Teva Czech Industries in the Czech Republic, and the product is manufactured for Teva Pharmaceuticals USA, Inc. The NDC code for these tablets is 50111-334-01, and the package contains 100 tablets. It is advised to refer to the package insert for full prescribing information and dosage instructions.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.