Telmisartan Tablet
Product Images NDC 65162-293

13 FDA label images from Amneal Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Telmisartan (NDC 65162-293). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

239f7255-figure-01 (Telmisartan Tablets Usp 1)

239f7255-figure-01 (Telmisartan Tablets Usp 1)
Chemical structure of telmisartan, showing its molecular framework with multiple aromatic rings, nitrogen atoms, and functional groups including a carboxylic acid group.*
FDA Label Image

10 (Telmisartan Tablets Usp 10)

10 (Telmisartan Tablets Usp 10)
Packaging label for Telmisartan 40 mg oral tablets by Amneal Pharmaceuticals Pvt. Ltd. The label includes multiple individual tablet blister labels with the text Telmisartan Tablet, USP, 40 mg, and a notice to remove from blister at time of use. Each label shows the NDC 65162-292-63 and includes space for lot number and expiration date.*
FDA Label Image

10 (Telmisartan Tablets Usp 11)

10 (Telmisartan Tablets Usp 11)
Label of Telmisartan Tablets USP, 80 mg, manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. The label indicates the package contains 30 tablets, oral dosage form, and includes storage instructions and warnings about moisture sensitivity. The label also features the NDC 65162-293-03 and a barcode.*
FDA Label Image

10 (Telmisartan Tablets Usp 12)

10 (Telmisartan Tablets Usp 12)
Telmisartan Tablets, USP 80 mg oral tablet label by Amneal Pharmaceuticals LLC. The label shows a blister pack of 30 tablets (3 x 10 unit-dose) with details including storage instructions, manufacturing and distribution information, and dosage advisory. The color scheme includes orange and white with the Amneal logo prominently displayed.*
FDA Label Image

10 (Telmisartan Tablets Usp 13)

10 (Telmisartan Tablets Usp 13)
Packaging label for Telmisartan 80 mg oral tablets by Amneal Pharmaceuticals Pvt. Ltd. The label includes black text on a white background featuring the product name, strength, dosage form, instructions to remove from blister at time of use, barcode, and placeholders for lot and expiration dates. Multiple identical labels are shown on a sheet for blister packaging.*
FDA Label Image

239f7255-figure-02 (Telmisartan Tablets Usp 2)

239f7255-figure-02 (Telmisartan Tablets Usp 2)
An instructional diagram showing a hand pushing a tablet through a blister pack. The image illustrates how to remove a tablet from the packaging by pressing on the tablet area to pop it out.*
FDA Label Image

239f7255-figure-03 (Telmisartan Tablets Usp 3)

239f7255-figure-03 (Telmisartan Tablets Usp 3)
An instructional illustration showing two hands peeling a foil blister label to reveal tablets underneath. The label includes text with the proprietary name Telmisartan and other product information, indicating this is for Telmisartan oral tablets in blister packaging.*
FDA Label Image

239f7255-figure-04 (Telmisartan Tablets Usp 4)

239f7255-figure-04 (Telmisartan Tablets Usp 4)
An instructional illustration showing a person using both hands to peel or open a foil-sealed container, with an arrow indicating the direction of peeling. The container likely holds tablets, consistent with medication packaging.*
FDA Label Image

10 (Telmisartan Tablets Usp 5)

10 (Telmisartan Tablets Usp 5)
Label for Telmisartan Tablets, USP 20 mg oral tablets by Amneal Pharmaceuticals LLC. The label states 30 tablets per bottle. It includes storage instructions, moisture sensitivity warnings, and manufacturer information, indicating the product is prescription only and manufactured by Amneal Pharmaceuticals Pvt. Ltd. in Ahmedabad, India.*
FDA Label Image

10 (Telmisartan Tablets Usp 6)

10 (Telmisartan Tablets Usp 6)
Telmisartan Tablets USP 20 mg blister package label by Amneal Pharmaceuticals LLC. The label shows the product name and strength prominently with the Amneal logo, notes 30 tablets in 3 x 10 unit-dose blister packs, and specifies manufacturing and distribution details for Amneal Pharmaceuticals Pvt. Ltd. and Amneal Pharmaceuticals LLC. Additional information includes storage temperature, a barcode, and child-resistant packaging notice.*
FDA Label Image

10 (Telmisartan Tablets Usp 7)

10 (Telmisartan Tablets Usp 7)
Blister card label for Telmisartan 20 mg oral tablets by Amneal Pharmaceuticals Pvt. Ltd. The label displays the product name, dosage strength (20 mg), dosage form (tablet, USP), and instructions to remove each tablet from the blister at time of use. Each tablet unit is individually marked with a barcode and NDC 65162-291-63.*
FDA Label Image

10 (Telmisartan Tablets Usp 8)

10 (Telmisartan Tablets Usp 8)
Drug facts label for Telmisartan Tablets, USP 40 mg from Amneal Pharmaceuticals LLC. The label details dosage instructions, storage conditions (20° to 25°C with excursions permitted), and moisture sensitivity warnings. It includes manufacturer information for Amneal Pharmaceuticals Pvt Ltd, India, and distributor details for Amneal Pharmaceuticals LLC, New Jersey. The label also shows the NDC number, a small image of a scored pink tablet, and bar code.*
FDA Label Image

30 (Telmisartan Tablets Usp 9)

30 (Telmisartan Tablets Usp 9)
Label for Telmisartan Tablets, USP 40 mg oral tablets by Amneal Pharmaceuticals LLC. Pack contains 30 tablets in a child-resistant blister package. Label includes storage instructions, manufacturer Amneal Pharmaceuticals Pvt. Ltd. in India, and distributor Amneal Pharmaceuticals LLC in New Jersey, USA.*

* 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.