Benztropine Mesylate Injection
Product Images NDC 0143-9233

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Benztropine Mesylate (NDC 0143-9233). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., 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

Chemical Structure (Benztropine Mesylate Injection Vial 1)

Chemical structure of Benztropine Mesylate showing its molecular framework including the tropane ring system and associated functional groups.*

FDA Label Image

Benztropine Mesylate Injection, Usp Container Label (Benztropine Mesylate Injection Vial 2)

Label for Benztropine Mesylate Injection, USP, 2 mg per 2 mL (1 mg/mL) single-dose vial. Intended for intravenous or intramuscular use, distributed by Hikma Pharmaceuticals USA Inc. Includes NDC 0143-9233-01. The label shows lot and expiration date fields.*

FDA Label Image

Benztropine Mesylate Injection, Usp Carton Label (Benztropine Mesylate Injection Vial 3)

Benztropine Mesylate Injection, USP 2 mg per 2 mL (1 mg/mL) label for intramuscular and intravenous use. Packaging shows a box containing 5 single-dose vials of 2 mL each. Labeled by Hikma Pharmaceuticals USA Inc. The label includes dosage information, NDC 0143-9233-05, and storage instructions.*

FDA Label Image

Representative Serialization Image (Benztropine Mesylate Injection Vial 4)

Label of Benztropine Mesylate injection 1 mg/mL by Hikma Pharmaceuticals USA Inc. The label includes a QR code and text fields indicating GTIN, serial number, expiration date, and lot number placeholders.*

* 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.