Benztropine Mesylate Tablet
Product Images NDC 69097-826

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Benztropine Mesylate (NDC 69097-826). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cipla 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

Benztropinemesylate 0.5mg 100c Cl

Label for Benztropine Mesylate Tablets USP 0.5 mg, oral tablet form, supplied by Cipla USA Inc. The label states the product is prescription only, contains 100 tablets, and includes dosage information and storage instructions. The label also shows the NDC code 69097-826-07 and a barcode.*

FDA Label Image

Benztropinemesylate 1mg 100c Cl

Label for Benztropine Mesylate Tablets, USP 1 mg oral tablets. The bottle contains 100 tablets. Label shows manufacturer details as Cipla USA Inc. and InvaGen Pharmaceuticals, Inc. Dosage information and storage instructions are partially provided, along with a barcode and QR code on the label.*

FDA Label Image

Benztropinemesylate 2mg 100c Cl

Label for Benztropine Mesylate Tablets, USP 2 mg, oral tablets. The label shows the product name, strength, and a total of 100 tablets in the container. It includes manufacturer information for Cipla USA, Inc. and InvaGen Pharmaceuticals, Inc., dosage instructions, storage recommendations, and a barcode section with identifiers.*

FDA Label Image

Benztropinemesylate Fig

Chemical structure of benztropine mesylate, showing its molecular framework including nitrogen-containing bicyclic ring and phenyl groups attached to the oxygen atom, along with the mesylate group (CH3SO3H).*

* 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.