Amlodipine, Valsartan And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 68180-772

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Amlodipine, Valsartan And Hydrochlorothiazide (NDC 68180-772). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

111922d9 0549 464b 8b1f D8240a5f7900 01

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 02

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 03

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 04

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 05

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 06

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 07

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 08

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 09

This is a description of a medication, but the only information provided is the NDC (National Drug Code) number, the dosage of Amlodipine and Hydrochlorothiazide, and storage instructions. There is no additional information about the medication, its uses or side effects.*

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 10

NDC 68180-772-06 is a prescription drug with Amlodipine, Valsartan, and Hydrochlorothiazide. It is available in film-coated tablets and is manufactured by Lupin Limited of Goa 403 722 in India for Lupin Pharmaceuticals in Baltimore, Maryland. Each tablet contains 10mg Amlodipine besylate USP equivalent to Amlodipine, 160mg Valsartan USP, and 12.5mg Hydrochlorothiazide USP. The complete dosing instructions can be found in the accompanying prescribing information. It should be stored at 25°C (77°F) with excursions permitted to 15°t0 30°C (59° to 86°F) and protected from moisture.*

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 11

This is a description of a prescription drug. The drug has the NDC number 68180-773-06 and is manufactured by Lupin Pharmaceuticals, Inc. It contains Amlodipine besylate USP equivalent to 5mg and Valsartan USP 160mg and Hydrochlorothiazide USP 25mg. Each tablet is film-coated and the package contains 30 tablets. It is recommended to store the drug between 15°C to 30°C (59°F to 86°F) and protect it from moisture. The accompanying prescribing information should be consulted for complete dosing instructions.*

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 12

This is a prescription drug called Amlodipine, Valsartan, and Hydrochlorothiazide Tablets USP manufactured by Lupin Limited in Goa, India. Each tablet contains Amlodipine besylate, Valsartan, and Hydrochlorothiazide, with a dosage of 10mg, 160mg, and 25mg, respectively. The enclosed prescribing information provides detailed dosing and administration instructions. The drug should be stored at room temperature between 15°C to 30°C, and protected from moisture. This drug should be kept away from the reach of children.*

FDA Label Image

111922d9 0549 464b 8b1f D8240a5f7900 13

This is a prescription drug with the NDC code 68180-775-06. It is a film-coated tablet that contains Amlodipine besylate USP equivalent to Amlodipine 10mg, Valsartan USP 320mg, and Hydrochlorothiazide USP 25mg. The manufacturer of this drug is Lupin Pharmaceuticals, Inc. The dosage information can be found in the accompanying prescribing information. The tablets should be stored at room temperature and protected from moisture. It is important to keep this drug out of the reach of children.*

* 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.