Valsartan Tablet, Film Coated
Product Images NDC 42385-990

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Valsartan (NDC 42385-990). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laurus Labs Limited, 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

Figure1 (Valsartan Figure1)

A forest plot chart comparing Valsartan versus Captopril across patient subgroups. It displays patient percentages in categories such as age (<65, ≥65), gender, race (Caucasian, Non-Caucasian), region (US, Non-US), and beta-blocker use, with markers and confidence intervals indicating the favorability towards Valsartan or Captopril.*

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Valsartan-figure10 (Valsartan Figure10)

Packaging label for Valsartan Tablets, USP 160 mg film-coated oral tablets by Laurus Labs Limited. The label indicates 100 unit-dose tablets in the package. Storage instructions specify controlled room temperature with protection from moisture. Manufacturer information is included for Laurus Generics Inc. and Laurus Labs Limited, India.*

FDA Label Image

Valsartan-figure11 (Valsartan Figure11)

Label for Valsartan Tablets, USP 320 mg, film-coated oral tablets. The package contains 30 tablets and is labeled as prescription only. Manufactured by Laurus Labs Limited and labeled for Laurus Generics Inc. Storage instructions specify controlled room temperature and moisture protection.*

FDA Label Image

Figure12 (Valsartan Figure12)

A sheet of multiple identical labels for Valsartan Tablet USP, each indicating a strength of 320 mg. Each label includes the NDC number 42385-992-10, the text 'Rx only,' manufacturer Laurus Labs Limited, and spaces for lot and expiration dates. Each label features a barcode.*

FDA Label Image

Valsartan-figure13 (Valsartan Figure13)

Box packaging label for Valsartan Tablets, USP 320 mg film-coated oral tablets. The box contains 100 unit-dose tablets (10 x 10) and is marked Rx only. Manufactured by Laurus Labs Limited and labeled for Laurus Generics Inc. Storage instructions and a child safety warning are included on the label.*

FDA Label Image

Valsartan-figure2 (Valsartan Figure2)

Label for Valsartan Tablets USP 40 mg film-coated tablets, containing 30 scored tablets. Manufactured by Laurus Labs Limited and labeled for Laurus Generics Inc. The label includes storage instructions, dosage reference, and barcode.*

FDA Label Image

Figure3 (Valsartan Figure3)

Sheet of ten identical Valsartan 40 mg film-coated tablet labels, each showing the product name, strength, dosage form, and manufacturer Laurus Labs Limited. The labels include barcode, NDC 42385-989-10, Rx only status, and blank spaces for lot and expiration dates.*

FDA Label Image

Valsartan-figure4.jpg (Valsartan Figure4)

Packaging label for Valsartan Tablets USP 40 mg, film-coated oral tablets. The label shows a package size of 100 unit-dose scored tablets (10 x 10). The product is labeled for prescription use only and is manufactured by Laurus Labs Limited, India, for Laurus Generics Inc. The label includes storage instructions and a barcode.*

FDA Label Image

Valsartan-figure5 (Valsartan Figure5)

Label for Valsartan Tablets, USP 80 mg oral film-coated tablets. The package contains 30 tablets. Manufactured by Laurus Labs Limited and labeled for Laurus Generics Inc. The label includes storage instructions and warnings to protect from moisture and keep out of reach of children. The NDC is 42385-990-30.*

FDA Label Image

Figure6 (Valsartan Figure6)

This image shows multiple repeating drug labels for Valsartan 80 mg film-coated tablets. Each label includes the proprietary name Valsartan, the dosage strength of 80 mg, and the designation Tablet, USP. The labels also display the NDC number 42385-990-10 and identify Laurus Labs Limited as the manufacturer. Lot number and expiration date fields are present but not filled in. A barcode is included on each label.*

FDA Label Image

Valsartan-figure7 (Valsartan Figure7)

This is the packaging label for Valsartan Tablets, USP 80 mg, film-coated oral tablets. The label indicates a quantity of 100 unit-dose tablets in a 10 x 10 configuration. It is labeled by Laurus Labs Limited and manufactured for Laurus Generics Inc. The label includes storage instructions and is marked Rx only.*

FDA Label Image

Valsartan-figure8 (Valsartan Figure8)

Label for Valsartan Tablets USP 160 mg, film-coated oral tablets supplied in a package of 30 tablets. The label includes storage instructions, manufacturer details for Laurus Labs Limited, and distributor information for Laurus Generics Inc. It displays the NDC number 42385-991-30 and includes a barcode and a Laurus Labs logo.*

FDA Label Image

Figure9 (Valsartan Figure9)

This image shows a sheet of ten identical pharmacy labels for Valsartan Tablet, USP 160 mg oral film-coated tablets. Each label includes the NDC number 42385-991-10, manufacturer Laurus Labs Limited, sections for lot and expiration date, and a barcode. The labels indicate the product is prescription-only (Rx only).*

FDA Label Image

Valsartan (Valsartan Structure)

Chemical structure of the active ingredient Valsartan, showing the molecular arrangement with various functional groups including carboxyl, amide, and tetrazole rings.*

* 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.