Zidovudine Capsule
Product Images NDC 65862-107

3 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zidovudine (NDC 65862-107). 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (100 mg (100 Capsules Bottle))

Package Label-principal Display Panel (100 mg (100 Capsules Bottle))
Label for Zidovudine Capsules USP 100 mg, a drug for further processing. The label states each capsule contains 100 mg of zidovudine USP and the package contains 100 capsules. It includes storage instructions, dispensing requirements, and distributor details for Aurobindo Pharma USA, Inc. The label also shows the NDC 65862-107-01 and notes the product is made in India by Aurobindo Pharma Limited.*
FDA Label Image

Package Label-principal Display Panel (100 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (100 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Zidovudine Capsules, USP 100 mg by Aurobindo Pharma Limited, NDC 65862-107. The label indicates the product contains 100 capsules (10 x 10 unit-dose) and is distributed by Aurobindo Pharma USA, Inc. The label notes child-resistance and storage conditions, with a barcode and manufacturing information from India.*
FDA Label Image

Chemical Structure (Zidovudine Str)

Chemical Structure (Zidovudine Str)
Chemical structure diagram of zidovudine, showing its molecular components and bonds as part of FDA labeling.*

* 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.