Telmisartan And Hydrochlorothiazide Tablet
Product Images NDC 68462-840

10 FDA label images from Glenmark Pharmaceuticals Inc., Usa · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Telmisartan And Hydrochlorothiazide (NDC 68462-840). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals Inc., Usa, 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
FDA Label Image
FDA Label Image

Micardis-hct-structure-01 (Micardis Hct Structure 01)

Micardis-hct-structure-01 (Micardis Hct Structure 01)
Chemical structure of Telmisartan, one of the active ingredients in Telmisartan and Hydrochlorothiazide tablets by Glenmark Pharmaceuticals Inc., USA.*
FDA Label Image

Micardis-hct-structure-02 (Micardis Hct Structure 02)

Micardis-hct-structure-02 (Micardis Hct Structure 02)
Chemical structure of Telmisartan, an active ingredient in the combination drug Telmisartan and Hydrochlorothiazide. The diagram shows the molecular framework with notable functional groups including a sulfonamide, chloride, and imidazole ring.*
FDA Label Image

Step1 (Step1)

Step1 (Step1)
An instructional illustration showing how to peel a blister card containing tablets of Telmisartan and Hydrochlorothiazide 40 mg / 12.5 mg. The image demonstrates fingers peeling back individual tablet compartments for oral tablets from Glenmark Pharmaceuticals Inc., USA.*
FDA Label Image

Step2 (Step2)

Step2 (Step2)
An instructional illustration showing hands demonstrating how to open a Telmisartan and Hydrochlorothiazide tablet unit dose package by tearing and peeling back the foil wrapper to access the tablet inside.*
FDA Label Image

Step3 (Step3)

Step3 (Step3)
Illustration showing hands opening a blister pack by pressing on a tablet through the foil backing. This instructional diagram demonstrates how to remove a tablet from its blister package.*
FDA Label Image

Telmisartan-hctz-tab-40mg-12-5mg (Telmisartan Hctz Tab 40mg 12 5mg)

Telmisartan-hctz-tab-40mg-12-5mg (Telmisartan Hctz Tab 40mg 12 5mg)
Packaging label for Telmisartan and Hydrochlorothiazide Tablets USP 40 mg/12.5 mg by Glenmark Pharmaceuticals Inc., USA. The label shows the product name, strength, quantity of 30 tablets (3x10 unit-dose), and manufacturer information including Glenmark Pharmaceuticals Ltd. India and Glenmark Pharmaceuticals Inc. USA. It includes storage instructions and a barcode.*
FDA Label Image

Telmisartan-hctz-tab-80mg-12-5mg (Telmisartan Hctz Tab 80mg 12 5mg)

Telmisartan-hctz-tab-80mg-12-5mg (Telmisartan Hctz Tab 80mg 12 5mg)
Packaging label for Telmisartan and Hydrochlorothiazide Tablets USP 80 mg/12.5 mg by Glenmark Pharmaceuticals Inc., USA. The oral tablet dose form contains 30 tablets in a 3x10 unit-dose package. The label includes dosage strength, manufacturer details, barcode, and storage instructions emphasizing moisture sensitivity.*
FDA Label Image

Telmisartan-hctz-tab-80mg-25mg (Telmisartan Hctz Tab 80mg 25mg)

Telmisartan-hctz-tab-80mg-25mg (Telmisartan Hctz Tab 80mg 25mg)
Packaging label for Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg strength, oral tablet form. The label shows the product name clearly with the dosage strength boxed in yellow. Manufactured by Glenmark Pharmaceuticals Ltd and Glenmark Pharmaceuticals Inc., USA. The package contains 30 tablets in 3x10 unit-dose blister packs. Additional instructions note the tablets are moisture sensitive and should not be removed from blisters until immediately before use.*

* 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.