Cimetidine Tablet, Film Coated
Product Images NDC 51655-697

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cimetidine (NDC 51655-697). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 697 51 Master Bottle Label Approval Rev A 03 21)

Label (51655 697 51 Master Bottle Label Approval   Rev A 03 21)
NDC: 51655-697-51 1 Cimetidine Tablets, USP 400 mg, 40 Tablets. It is Rx Only. The dosage information is available in the package insert. Store at 20° - 25°C (687 - 77°F) (See USP Controlled Room Temperature). Keep out of the reach of children and store in the original container. Protect from light and keep the container tightly closed. It has been repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46203. GTIN: 0035165569751. Each film-coated tablet contains Cimetidine. The S/N is not available for review. The expiry date and lot number of the Mylan Pharmaceuticals Inc. are both 0000000000.*
FDA Label Image

Structural Formula (F45db833 Cec2 45d8 8b5f Ca1e820b8f48 01)

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