Ranitidine
Product Images NDC 33261-099

3 FDA label images from Aidarex Pharmaceuticals Llc · 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 Ranitidine (NDC 33261-099). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals 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

Click To Zoom In (Ranitadine Tabs Amneal 1)

Click To Zoom In (Ranitadine Tabs Amneal 1)
Chemical structure of ranitidine hydrochloride, showing the molecular arrangement with a furan ring and a nitroguanidine moiety linked by a sulfide group.*
FDA Label Image

Ranitidine Tablet (Ranitadine Tabs Amneal 2)

Ranitidine Tablet (Ranitadine Tabs Amneal 2)
Ranitidine USP 300 mg tablets packaging label by Aidarex Pharmaceuticals LLC. The label indicates 30 tablets per package, with equivalent ranitidine hydrochloride content of 334.8 mg per 300 mg ranitidine tablet. It includes lot number, distributor information (Zantac, Bridgewater, NJ), and dosing directions to take every specified hours as directed. The label also shows NDC numbers and package identification codes.*
FDA Label Image

Ranitidine Tablet (Ranitadine Tabs Amneal 3)

Ranitidine Tablet (Ranitadine Tabs Amneal 3)
Ranitidine USP 150 mg tablet bottle label from Aidarex Pharmaceuticals LLC. The label indicates a package of 20 tablets, with directions to take as prescribed. The label includes lot number, expiration date, and distributor address in Bridgewater, NJ. The label highlights Ranitidine hydrochloride equivalent to 150 mg ranitidine per tablet.*

* 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.