Amlodipine Besylate Tablet
Product Images NDC 65841-620

3 FDA label images from Zydus Lifesciences 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 Amlodipine Besylate (NDC 65841-620). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences 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

Amlodipine Besylate Tablets Usp, 2.5 mg (6346c397 7d13 49d9 8e0b 53c0ae5f09e0 01)

Amlodipine Besylate Tablets Usp, 2.5 mg (6346c397 7d13 49d9 8e0b 53c0ae5f09e0 01)
Label for Amlodipine Besylate Tablets USP, 2.5 mg strength, oral tablet form. The packaging indicates 90 tablets with prescription-only status. Manufactured by Zydus Lifesciences Limited, India. The label includes dosage storage instructions and a barcode on the left side along with the NDC number 65841-620-16.*
FDA Label Image

Amlodipine Besylate Tablets Usp, 5 mg (6346c397 7d13 49d9 8e0b 53c0ae5f09e0 02)

Amlodipine Besylate Tablets Usp, 5 mg (6346c397 7d13 49d9 8e0b 53c0ae5f09e0 02)
Amlodipine Besylate Tablets, USP 5 mg oral tablets label by Zydus Lifesciences Limited. The package contains 90 tablets with an Rx only designation. The label includes storage instructions, dosage reference, and manufacturer details. The NDC code shown is 65841-621-16.*
FDA Label Image

Amlodipine Besylate Tablets Usp, 10 mg (6346c397 7d13 49d9 8e0b 53c0ae5f09e0 03)

Amlodipine Besylate Tablets Usp, 10 mg (6346c397 7d13 49d9 8e0b 53c0ae5f09e0 03)
Amlodipine Besylate Tablets, USP 10 mg oral tablet label from Zydus Lifesciences Limited. The label indicates a package size of 90 tablets and includes storage instructions, dosage reference to package insert, a barcode, and manufacturer information. The NDC code shown is 65841-622-16.*

* 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.