Amlodipine And Valsartan Tablet
Product Images NDC 68180-766

18 FDA label images from Lupin Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Amlodipine And Valsartan (NDC 68180-766). 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

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 01

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 01
A line graph showing the percentage of systolic blood pressure (SBP) below 140 mmHg plotted against baseline SBP (mmHg). The graph compares four groups: Amlodipine and Valsartan tablets 10/320 mg, Valsartan 320 mg, Amlodipine 10 mg, and placebo, indicating their efficacy in lowering SBP across different baseline values.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 02

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 02
A line graph depicting the percentage of patients with diastolic blood pressure (DBP) under 90 mmHg versus baseline DBP (mmHg). The graph compares effects of Amlodipine and Valsartan tablets 10/320 mg, Valsartan 320 mg, Amlodipine 10 mg, and placebo, with each treatment represented by a different marker shape and line style.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 03

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 03
A line chart showing the percentage of systolic blood pressure (SBP) readings below 130 mmHg compared to baseline SBP measurements (140 to 180 mmHg). Four groups are presented: Amlodipine and Valsartan tablets 10/320 mg, Valsartan 320 mg, Amlodipine 10 mg, and Placebo, with corresponding trend lines indicating response rates by baseline SBP values.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 04

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 04
Line graph comparing the percentage of diastolic blood pressure (DBP) less than 80 mmHg across different baseline DBP values (95 to 110 mmHg). It includes data for Amlodipine and Valsartan Tablets 10/320 mg, Valsartan 320 mg, Amlodipine 10 mg, and placebo as indicated by different symbols in the legend.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 05

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 05
Chemical structure of the active ingredients in Amlodipine and Valsartan, showing their molecular formulas with various chemical groups and bonds depicted.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 06

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 06
Chemical structure of the active ingredient Amlodipine and Valsartan depicted in a molecular diagram showing the arrangement of atoms and bonds.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 07

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 07
Label for Amlodipine and Valsartan Tablets USP, 5 mg/160 mg strength, oral tablet dosage form. The label states Rx only, contains 30 tablets, and is manufactured by Lupin Pharmaceuticals, Inc. It lists the active ingredients and their amounts per tablet, storage instructions, and manufacturing details including Lupin Limited in India.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 08

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 08
Packaging label for Amlodipine and Valsartan Tablets USP 5 mg/160 mg by Lupin Pharmaceuticals, Inc. The label includes NDC 68180-764-13 and indicates 100 tablets (10 x 10 Units-Dose). The label provides active ingredient strengths and storage instructions, with manufacturing information for Lupin Pharmaceuticals, Baltimore, MD, and Lupin Limited, Goa, India.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 09

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 09
Label for Amlodipine and Valsartan Tablet USP, strength 5 mg/160 mg. Oral tablet manufactured for Lupin Pharmaceuticals, Inc. The label includes the NDC 68180-764-11, barcode, and space for lot number and expiration date. The label is repeated multiple times on the sheet.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 10

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 10
Label for Amlodipine and Valsartan Tablets USP with strengths 10 mg/160 mg, provided in a 30 tablet package. The label shows the product is manufactured by Lupin Pharmaceuticals, Inc., with storage instructions and barcode. It also includes details for manufacturing in India by Lupin Limited.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 11

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 11
Packaging label for Amlodipine and Valsartan Tablets USP, 10 mg/160 mg strength, oral tablet form. The label shows the product name prominently with the strength below it. The package contains 100 tablets (10 x 10 units-dose) and is labeled Rx only. Manufactured for Lupin Pharmaceuticals, Inc., the label indicates storage instructions and includes a barcode and NDC 68180-765-13.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 12

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 12
A sheet of multiple identical packaging labels for Amlodipine and Valsartan Tablet USP 10 mg/160 mg. Each label includes the proprietary and generic names, dosage strength, manufacturer Lupin Pharmaceuticals, Inc., NDC 68180-765-11, and barcode. The label states Rx only and provides space for lot number and expiration date.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 13

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 13
Amlodipine and Valsartan Tablets USP 5 mg/320 mg oral tablet packaging label for 30 tablets. The label states the active ingredients as amlodipine besylate equivalent to 5 mg amlodipine and 320 mg valsartan. It includes storage instructions and manufacturer details for Lupin Pharmaceuticals, Inc., Baltimore, Maryland, and Lupin Limited, India.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 14

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 14
Packaging label for Amlodipine and Valsartan Tablets USP 5 mg/320 mg oral tablets by Lupin Pharmaceuticals, Inc. The package contains 100 tablets (10 x 10 units-dose) with NDC 68180-766-13. The label includes storage instructions and manufacturing details for Lupin Pharmaceuticals, Inc. in Maryland and Lupin Limited, India.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 15

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 15
Label sheet displaying multiple identical labels for Amlodipine and Valsartan Tablet USP, 5 mg/320 mg strength. Each label shows the proprietary and generic names, dosage strength, route as oral tablets, Rx-only status, manufacturer Lupin Pharmaceuticals, Inc., and includes NDC 68180-766-11. Barcodes and spaces for lot number and expiration date are also visible.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 16

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 16
Label of Amlodipine and Valsartan Tablets USP, strength 10 mg/320 mg, oral tablet form. The label indicates 30 tablets per package, manufactured by Lupin Pharmaceuticals, Inc., with storage instructions and barcode visible. The label also notes the product is Rx only.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 17

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 17
Packaging label for Amlodipine and Valsartan Tablets USP 10 mg/320 mg oral tablets by Lupin Pharmaceuticals, Inc. The label shows the product name, strength, prescription status (Rx only), package quantity of 100 tablets (10 x 10 units-dose), manufacturer details, and storage instructions. The design includes red, yellow, and green color accents with the labeler Lupin identified on front panels.*
FDA Label Image

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 18

84071e7c 54b0 4db3 9467 F6c2ba2f8c3b 18
Labels for Amlodipine and Valsartan Tablet USP 10 mg/320 mg manufactured by Lupin Pharmaceuticals, Inc. Each label includes the product name, strength, Rx only indication, manufacturer details, NDC 68180-767-11, barcode, and space for lot number and expiration date. The labels are arranged in a sheet format with identical repeat designs.*

* 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.