Benztropine Mesylate Injection
Product Images NDC 68382-860

3 FDA label images from Zydus Pharmaceuticals Usa Inc. · 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 Benztropine Mesylate (NDC 68382-860). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus 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.

Product Images & Figures Index

FDA Label Image

Benztropine-fig-01 (C4849b63 A84f 4cf0 B937 7ca4b33f2d25 01)

Benztropine-fig-01 (C4849b63 A84f 4cf0 B937 7ca4b33f2d25 01)
Chemical structure of benztropine mesylate, showing its bicyclic tropane ring system connected to ester and diphenyl groups, with a methanesulfonic acid component as indicated by the •CH3SO3H notation.*
FDA Label Image

Vial-label (C4849b63 A84f 4cf0 B937 7ca4b33f2d25 02)

Vial-label (C4849b63 A84f 4cf0 B937 7ca4b33f2d25 02)
Label for Benztropine Mesylate Injection, USP, 1 mg/mL (2 mg/2 mL) in a 2 mL single dose vial. Intended for intravenous or intramuscular use. Distributed by Zydus Pharmaceuticals USA Inc., Pennington, NJ. The label includes storage instructions and space for lot and expiration dates.*
FDA Label Image

Carton-label (C4849b63 A84f 4cf0 B937 7ca4b33f2d25 03)

Carton-label (C4849b63 A84f 4cf0 B937 7ca4b33f2d25 03)
Packaging label for Benztropine Mesylate Injection, USP, 2 mg/2 mL (1 mg/mL) injection solution. The label specifies use for intravenous or intramuscular administration and includes the labeler, Zydus Pharmaceuticals USA Inc. The package contains 5 single-dose vials of 2 mL each. Storage instructions and inactive ingredients are also listed.*

* 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.