Benztropine Mesylate Tablet
Product Images NDC 62135-141

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Benztropine Mesylate (NDC 62135-141). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, Llc., 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

Benztropine Mesylate Chemical Structure (Benztropine Mesylate Tablets 01)

Chemical structure diagram of Benztropine mesylate showing the molecular arrangement including a tropane nitrogen component and mesylate group (CH3SO3H).*

FDA Label Image

Principal Display Panelndc 62135-144-01benztropinemesylatetablets, Usp1 mgrx Only100 Tablets (Benztropine Mesylate Tablets 02)

Benztropine Mesylate 1 mg oral tablets label from Chartwell RX, LLC. The label states the product contains 100 tablets, is prescription only, and details storage instructions. It includes dosage directions and safety warnings, with NDC 62135-144-01 visible. The label features a blue and red design with the Chartwell Rx logo.*

FDA Label Image

Principal Display Panelndc 62135-144-10benztropinemesylatetablets, Usp1 mgrx Only1000 Tablets (Benztropine Mesylate Tablets 03)

Label for Benztropine Mesylate Tablets USP, 1 mg strength. The label shows 1000 tablets in the package, with prescription use only. It is manufactured by Chartwell RX, LLC. The label includes storage instructions and warnings to keep medications out of reach of children. The packaging features a red and blue design with the Chartwell Rx logo.*

FDA Label Image

Principal Display Panelndc 62135-142-01benztropinemesylatetablets, Usp2 mgrx Only100 Tablets (Benztropine Mesylate Tablets 04)

Label for Benztropine Mesylate Tablets, USP 2 mg oral tablets, containing 100 tablets per bottle. The label includes the NDC number 62135-142-01, marked Rx Only, and is manufactured by Chartwell RX, LLC. Label features a blue and purple color scheme with dosing information, warnings, and barcodes.*

FDA Label Image

Principal Display Panelndc 62135-142-10benztropinemesylatetablets, Usp2 mgrx Only1000 Tablets (Benztropine Mesylate Tablets 05)

Label for Benztropine Mesylate USP tablets, 2 mg strength, manufactured by Chartwell RX, LLC. The label states the product contains 1000 tablets, is prescription only, and includes storage instructions and handling precautions. Manufacturer and barcode details are visible.*

FDA Label Image

Benztropine Mesylate Tablets 06

Label for Benztropine Mesylate 1 mg tablets, USP, oral dosage form, in a bottle containing 180 tablets. The label states Rx Only and is manufactured by Chartwell RX, LLC. The packaging includes handling instructions, storage conditions, and safety warnings, with a barcode and the text 'No Varnish' on the side.*

FDA Label Image

Benztropine Mesylate Tablets 07

Label for Benztropine Mesylate Tablets, USP 2 mg by Chartwell RX, LLC. The bottle contains 180 oral tablets. The label includes storage instructions, dosage warnings, barcode, and identifying text indicating prescription only.*

FDA Label Image

Benztropine Mesylate Tablets 08

Label for Benztropine Mesylate Tablets, USP 1 mg oral tablets, manufactured by Chartwell RX, LLC. The label indicates Rx only and a package size of 540 tablets. Storage instructions and dosage information for Parkinsonism are included. The label also features the NDC number 62135-144-57 and a barcode.*

FDA Label Image

Benztropine Mesylate Tablets 09

Label for Benztropine Mesylate Tablets, USP 2 mg oral tablets by Chartwell RX, LLC. The label indicates a bottle of 540 tablets, prescription only, with storage instructions and a barcode. The strength is prominently displayed as 2 mg.*

* 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.