Meprobamate
Product Images NDC 55111-641

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Meprobamate (NDC 55111-641). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddy's Laboratories 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

200-100 (200 100)

Meprobamate 200 mg tablets packaging label from Dr. Reddy's Laboratories Limited, showing the NDC 55111-640-01. The label includes a white and blue design with dosage strength and a barcode. The package indicates that it contains 100 tablets for prescription use only.*

FDA Label Image

200-1000 (200 1000)

Meprobamate Tablets USP 200 mg packaged by Dr. Reddy's Laboratories Limited. The label indicates a bottle containing 1000 tablets with NDC 55111-640-10. Instructions for dosage and storage are provided, including storing at 20-25°C and dispensing in a well-closed container. The label also includes regulatory information and a barcode.*

FDA Label Image

400-100 (400 100)

Meprobamate 400 mg tablets USP label from Dr. Reddy's Laboratories Limited. The label indicates a package of 100 tablets for prescription use only. It includes dosage and storage instructions, a barcode, and lot and expiration date fields.*

FDA Label Image

400-500 (400 500)

Meprobamate 400 mg Tablets USP packaging label from Dr. Reddy's Laboratories Limited. The label shows a bottle containing 500 tablets, with dosage, storage instructions, and manufacturer details. The NDC code 55111-641-05 and image of bar code are also visible.*

FDA Label Image

Structure (Structure)

Chemical structure of meprobamate showing its molecular components and bonding arrangement.*

* 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.