Allopurinol Tablet
Product Images NDC 14445-170

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Allopurinol (NDC 14445-170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Indoco Remedies 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

Allopurinol-struct (Allopurinol Struct)

Allopurinol-struct (Allopurinol Struct)
Chemical structure of allopurinol, the active ingredient depicted as a heterocyclic compound with nitrogen atoms in the rings.*
FDA Label Image

Allop-100mg-100-tablets (Allop 100mg 100 Tablets)

Allop-100mg-100-tablets (Allop 100mg 100 Tablets)
Label for Allopurinol Tablets USP 100 mg, oral tablets in a package of 100. The label includes the NDC 14445-170-01, indicates prescription use, and shows the manufacturer as Indoco Remedies Limited, Goa, India. The label also provides storage instructions and includes a barcode and regulatory information.*
FDA Label Image

Allop-100mg-1000-tablets (Allop 100mg 1000 Tablets)

Allop-100mg-1000-tablets (Allop 100mg 1000 Tablets)
Label for Allopurinol Tablets, USP 100 mg oral tablets by Indoco Remedies Limited. The label indicates 1000 tablets in the container and includes storage instructions at controlled room temperature (68° to 77°F). It also mentions dispensing in a tight container and refers to the package insert for usage details. The label features a barcode and the Indoco logo.*
FDA Label Image

Allop-100mg-30-tablets (Allop 100mg 30 Tablets)

Allop-100mg-30-tablets (Allop 100mg 30 Tablets)
Allopurinol Tablets USP 100 mg oral tablets in a 30-count package by Indoco Remedies Limited. The label includes NDC 14445-170-30, storage instructions at 20° to 25°C, and a barcode. Manufactured in Verna, Goa, India. The label features the Indoco logo and a pharma code box.*
FDA Label Image

Allop-100mg-500-tablets (Allop 100mg 500 Tablets)

Allop-100mg-500-tablets (Allop 100mg 500 Tablets)
Label for Allopurinol Tablets USP 100 mg, oral tablets supplied in a container of 500 tablets. The label indicates the product is manufactured by Indoco Remedies Ltd, located in Verna, Goa, India. Storage instructions specify keeping the product between 20° to 25°C in a dry place and out of reach of children.*
FDA Label Image

Allop-300mg-100-tablets (Allop 300mg 100 Tablets)

Allop-300mg-100-tablets (Allop 300mg 100 Tablets)
Label for Allopurinol Tablets, USP 300 mg, oral tablets in a 100-count package by Indoco Remedies Limited. The label includes storage instructions at 20 to 25°C, dispensing information, and manufacturer details from Verna, Goa, India. The label also displays the NDC code 14445-171-01 and a barcode.*
FDA Label Image

Allop-300mg-1000-tablets (Allop 300mg 1000 Tablets)

Allop-300mg-1000-tablets (Allop 300mg 1000 Tablets)
Label for Allopurinol Tablets USP 300 mg, available in a package of 1000 tablets. The label features storage instructions to keep at 20° to 25°C in a dry place and directs dispensing in a tight container. Manufactured by Indoco Remedies Ltd., Verna, Goa, India. The label also displays the NDC 14445-171-00 and barcode.*
FDA Label Image

Allop-300mg-500-tablets (Allop 300mg 500 Tablets)

Allop-300mg-500-tablets (Allop 300mg 500 Tablets)
Label for Allopurinol Tablets, USP 300 mg oral tablets, container of 500 tablets. The label includes storage instructions at controlled room temperature and specifies dispensing in a tight container as per USP. Manufactured by Indoco Remedies Ltd., Verna Industrial Area, Goa, India. NDC 14445-171-05 is visible along with a barcode and the Indoco logo.*

* 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.