Meclizine Hydrochloride Tablet
Product Images NDC 60687-730

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Meclizine Hydrochloride (NDC 60687-730). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp73001

Meclizine Hydrochloride oral tablet, yellow, oval-shaped, debossed with imprint 'AN 442' on one side and blank on the other. No other markings or imprints visible. Scale in millimeters shown around the tablets.*

FDA Label Image

25 mg Meclizine Hydrochloride Tablet Blister (Blister)

Label sheet for Meclizine Hydrochloride Tablets, USP 25 mg by American Health Packaging. Each label shows the product strength (25 mg), dosage form (tablet), lot number (1234567 or 123456), and expiration dates (02/23 or 03/17). Labels include barcodes and manufacturer information, arranged in a grid format.*

FDA Label Image

25 mg Meclizine Hydrochloride Tablets Carton (Carton)

Label for Meclizine Hydrochloride 25 mg tablets, USP, oral dosage form by American Health Packaging. The label indicates a package containing 100 tablets (10 blister packs of 10 each). It includes the NDC number 60687-730-01 and notes prescription-only status. Additional dosing and storage guidance are partially visible on the label.*

FDA Label Image

Structural Formula (Structure)

Chemical structure diagram of Meclizine Hydrochloride showing its molecular arrangement and chemical bonds as part of the compound's formula.*

* 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.