Diazepam Tablet
Product Images NDC 59651-653

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diazepam (NDC 59651-653). 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

Fig1 (Diazepam Fig1)

Label for Diazepam Tablets USP 2 mg oral tablets, containing 100 tablets per container. The label includes storage instructions, pharmacist guidance, and distributor information for Aurobindo Pharma USA, Inc. It also features the drug's NDC number 59651-652-01 and a barcode. The product is made in India by Aurobindo Pharma Limited.*

FDA Label Image

Fig2 (Diazepam Fig2)

Label for Diazepam Tablets, USP 5 mg oral tablets by Aurobindo Pharma USA, Inc. The label states NDC 59651-653-01, prescription only, 100 tablets per container. It includes storage instructions, medication guide directions, manufacturer details from India, and a barcode on the right side.*

FDA Label Image

Fig3 (Diazepam Fig3)

Label for Diazepam Tablets, USP 10 mg oral tablets by Aurobindo Pharma Limited. The label indicates 100 tablets per container with instructions to dispense the medication guide. It lists storage conditions, distributor information for Aurobindo Pharma USA, Inc., and notes the product is made in India. NDC 59651-654-01 is displayed along with a barcode.*

FDA Label Image

Chemical Structure (Diazepam Str)

Chemical structure diagram of diazepam, showing its molecular composition and bond arrangement. The image depicts the characteristic benzodiazepine ring with chlorine substitution and other chemical groups relevant to diazepam's structure.*

* 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.