Telmisartan And Hydrochlorothiazide Tablet
Product Images NDC 70756-316

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Telmisartan And Hydrochlorothiazide (NDC 70756-316). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma 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

Structure1 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 01)

Structure1 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 01)
Chemical structure diagram of the active ingredient telmisartan, showing its molecular arrangement with labeled atoms including nitrogen, carbon, oxygen, and hydrogen.*
FDA Label Image

Struct2 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 02)

Struct2 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 02)
Chemical structure diagram of hydrochlorothiazide, showing the molecular arrangement including sulfonamide, chlorine, and nitrogen-containing rings.*
FDA Label Image

Fig01 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 03)

Fig01 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 03)
An instructional illustration showing a hand opening a blister pack of tablets by peeling back the foil from the plastic cavity containing one tablet, with an arrow indicating the direction to lift the foil.*
FDA Label Image

Fig02 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 04)

Fig02 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 04)
An instructional diagram depicting hands opening a folded carton or packaging by lifting a flap. This type of image commonly illustrates how to access the contents of a medication carton for oral tablets.*
FDA Label Image

Fig03 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 05)

Fig03 (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 05)
An instructional illustration showing a hand using a thumb to press and push a tablet out of a blister pack. An arrow above the tablet indicates the pressing direction to release the tablet from the packaging.*
FDA Label Image

40-12.5 mg Bottle (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 06)

40-12.5 mg Bottle (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 06)
Label for Telmisartan and Hydrochlorothiazide Tablets USP, 40 mg/12.5 mg, oral tablet. The label states the product is moisture sensitive and should not be removed from the bottle until administration. It contains 30 tablets and is manufactured by Lifestar Pharma LLC in Mahwah, NJ, made in India. Storage instructions and dosage information reference accompanying prescribing information.*
FDA Label Image

80-12.5mg Bottle (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 07)

80-12.5mg Bottle (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 07)
Label for Telmisartan and Hydrochlorothiazide Tablets, USP 80 mg/12.5 mg oral tablets in a 30-tablet bottle by Lifestar Pharma LLC. The label notes the product is moisture sensitive and includes storage instructions, dosage form, and the manufacturer details including the address and country of manufacture.*
FDA Label Image

80-25mgbottle (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 08)

80-25mgbottle (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 08)
Label for Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, oral tablets. The package contains 30 tablets and is labeled by Lifestar Pharma LLC. It notes the tablets are moisture sensitive and includes storage instructions and manufacturing details, including that it is made in India.*
FDA Label Image

40-12.5mg 30 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 09)

40-12.5mg 30 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 09)
Packaging label for Telmisartan and Hydrochlorothiazide Tablets USP containing 40 mg telmisartan and 12.5 mg hydrochlorothiazide per tablet. The label indicates it is moisture sensitive, provided in blister packs of 30 tablets (3 x 10 unit-dose), and labeled for prescription use only. Manufactured by Lifestar Pharma LLC, the label includes storage instructions and barcode.*
FDA Label Image

80-12.5mg 30 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 10)

80-12.5mg 30 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 10)
Label for Telmisartan and Hydrochlorothiazide Tablets, USP, 80 mg/12.5 mg per tablet oral tablets. The label shows the product strength, manufacturer Lifestar Pharma LLC, and a package count of 30 tablets (3 x 10 unit-dose). It includes storage instructions and a barcode, with the product made in India.*
FDA Label Image

80-25mg 30 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 11)

80-25mg 30 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 11)
Packaging label for Telmisartan and Hydrochlorothiazide Tablets, USP, 80 mg/25 mg per tablet. The rectangular label shows the product name and strength prominently, with a patient warning about moisture sensitivity and storage instructions. The labeled package contains 30 tablets (3 x 10 unit-dose) and is distributed by Lifestar Pharma LLC. A barcode and manufacturing details indicating production in India are also visible.*
FDA Label Image

40-12.5 mg 100 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 12)

40-12.5 mg 100 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 12)
Label for Telmisartan and Hydrochlorothiazide Tablets USP, each tablet containing 40 mg of telmisartan and 12.5 mg of hydrochlorothiazide. The label includes storage instructions, manufacturer information (Lifestar Pharma LLC), package size of 100 tablets, and a barcode. The product is oral tablets indicated as prescription only.*
FDA Label Image

80-12.5 mg 100 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 13)

80-12.5 mg 100 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 13)
Label for Telmisartan and Hydrochlorothiazide Tablets, USP, 80 mg/12.5 mg per tablet, oral tablets. The packaging indicates 100 tablets (10 x 10 unit-dose) and states the product is moisture sensitive and prescription only. Manufactured for Lifestar Pharma LLC, Mahwah, NJ, made in India, with an NDC of 70756-316-99.*
FDA Label Image

80-25mg 100 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 14)

80-25mg 100 Carton (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 14)
Label for Telmisartan and Hydrochlorothiazide Tablets USP, containing 80 mg telmisartan and 25 mg hydrochlorothiazide per tablet. Oral tablet form in a package of 100 tablets (10 x 10 unit-dose), labeled Rx only. Manufactured by Lifestar Pharma LLC, with storage instructions and a barcode shown.*
FDA Label Image

40-12.5mg Foil (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 15)

40-12.5mg Foil (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 15)
Carton label for Telmisartan and Hydrochlorothiazide Tablets, USP, 40 mg/12.5 mg oral tablets. The label includes usage instructions to remove tablets from blister at time of use. Manufactured by Lifestar Pharma LLC, Mahwah, NJ 07430, it features barcodes, lot number, expiration date fields, and is marked Rx only. The label is designed for multiple tablets in blister packaging.*
FDA Label Image

80-12.5 mg Foil (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 16)

80-12.5 mg Foil (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 16)
Packaging label for telmisartan and hydrochlorothiazide tablets, USP, with a strength of 80 mg/12.5 mg. The label shows multiple imprints including dosage strength in magenta, manufacturer Lifestar Pharma LLC located in Mahwah, NJ, and instructions to remove tablets from blister at time of use. The label includes barcode, lot number, expiration date, and NDC information.*
FDA Label Image

80-25 mg Foil (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 17)

80-25 mg Foil (E2e37d28 F6a3 4ab2 90ee 23b058d68dcf 17)
Blister card packaging label for Telmisartan and Hydrochlorothiazide Tablets, USP, 80 mg/25 mg strength. The label includes dosage instructions to remove from the blister at time of use. Manufactured by Lifestar Pharma LLC, Mahwah, NJ. Each tablet is marked with the product name, strength, barcode, lot, and expiration date placeholders.*

* 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.