Meclizine Hydrochloride Tablet
Product Images NDC 0904-7375

View Photos of 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 Meclizine Hydrochloride (NDC 0904-7375). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

Carton Label 25 mg (F99f13ab 33c0 4304 8dc5 3a75f3909377 00)

Carton Label 25 mg (F99f13ab 33c0 4304 8dc5 3a75f3909377 00)
The image shows the packaging label for Meclizine Hydrochloride Tablets, USP 25 mg by Major Pharmaceuticals. It is a unit dose package containing 100 oral tablets (10 x 10). The label includes dosage strength, NDC 0904-7376-61, and limited usage instructions indicating the product is by prescription only and intended for institutional use only.*
FDA Label Image

Carton Label 12.5 mg (Image 01)

Carton Label 12.5 mg (Image 01)
Meclizine Hydrochloride 12.5 mg oral tablets by Major Pharmaceuticals. The label indicates unit dose packaging with a total of 100 tablets (10 x 10). It includes dosing instructions, storage conditions, and warnings. The label also shows NDC 0904-7375-61 and states the product is Rx only and intended for institutional use.*
FDA Label Image

Structural Formula (Meclizine Hydrochloride Tablets Usp India 1)

Structural Formula (Meclizine Hydrochloride Tablets Usp India 1)
Chemical structure of Meclizine Hydrochloride, illustrating its molecular composition including chlorine, nitrogen-containing rings, and methyl groups, along with its hydrate form (2HCl.H2O).*

* 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.