Valsartan Tablet, Film Coated
Product Images NDC 55111-734

9 FDA label images from Dr. Reddy's Laboratories Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Valsartan (NDC 55111-734). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories 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

Carton1 (Carton1)

Carton1 (Carton1)
Packaging label for Valsartan Tablets USP, 40 mg film-coated tablets in a box containing 100 scored tablets (10 x 10 unit dose). The label shows the name, strength, dosage form, labeler Dr. Reddy's Laboratories Limited, and storage instructions. It includes the NDC 55111-731-78 and indicates manufacturing in India.*
FDA Label Image

Carton2 (Carton2)

Carton2 (Carton2)
Packaging label for Valsartan Tablets USP, 80 mg, film-coated oral tablets by Dr. Reddy's Laboratories Limited. The box contains 100 Unit Dose Tablets (10 blisters of 10 tablets each). The label includes storage instructions, dosage mention to refer package insert, and child safety warnings. Distributed by Dr. Reddy's Laboratories Inc., Princeton, NJ, made in India.*
FDA Label Image

Carton3 (Carton3)

Carton3 (Carton3)
Packaging label for Valsartan Tablets USP 160 mg, film-coated oral tablets by Dr. Reddy's Laboratories Limited. The carton indicates 100 unit dose tablets in 10 blister cards of 10 tablets each. Storage instructions and warnings appear on the box, along with labeling details including the NDC number and distributor location in Princeton, NJ. Made in India.*
FDA Label Image

Container1 (Container1)

Container1 (Container1)
Packaging label for Valsartan Tablets USP 40 mg film-coated tablets by Dr. Reddy's Laboratories Limited. The label indicates a package containing 30 scored tablets, with storage instructions and a barcode. It notes the product is prescription-only and includes the NDC 55111-731-30.*
FDA Label Image

Container2 (Container2)

Container2 (Container2)
Packaging label for Valsartan Tablets USP 80 mg film-coated tablets by Dr. Reddy's Laboratories Limited. The label indicates a package of 90 tablets with usage instructions and storage information. The design features a red semicircle element to the left and includes a barcode and NDC 55111-732-90.*
FDA Label Image

Container3 (Container3)

Container3 (Container3)
Label for Valsartan Tablets, USP 160 mg film-coated tablets by Dr. Reddy's Laboratories Limited. The label states a package insert is included, storage conditions (20°C to 25°C), and warnings to protect from moisture and keep out of reach of children. The package contains 90 tablets. Includes barcode, NDC 55111-733-90.*
FDA Label Image

Container4 (Container4)

Container4 (Container4)
Label for Valsartan Tablets, USP 320 mg film-coated tablets. The package contains 90 tablets and is labeled for Rx only. Manufactured by Dr. Reddy's Laboratories Limited, the label includes dosage storage instructions, lot number, barcode, and states the product is made in India.*
FDA Label Image

Figure (Figure)

Figure (Figure)
A forest plot comparing Valsartan versus Captopril across various patient subgroups, including age, gender, race, geographic location, and beta-blocker use. The horizontal axis represents the relative favoring of Valsartan or Captopril, with data points and confidence intervals shown for each subgroup.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of valsartan, showing its molecular arrangement with distinct rings, side chains, and functional groups as part of the compound's chemical formula.*

* 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.