Amlodipine Besylate Tablet
Product Images NDC 68180-721

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 68180-721). 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

Afcca25d 0e19 4800 A55d 1714067a4400 01

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 02

The text describes the results of a Kaplan-Meier analysis comparing the clinical outcomes of a medication named Amlodipine versus Placebo. It provides relevant statistical values such as the P-value, hazard ratio, and 95% confidence interval. The figure shows the composite clinical outcomes of both treatments over a period of 24 months. However, some characters are not readable in the text.*

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 03

This appears to be a table or chart displaying results from a study comparing the effects of Amlodipine versus Placebo. The information includes patient data such as gender, baseline blood pressure readings, and vessel disease status. It also includes hazard ratios with confidence intervals. Without additional context, it is difficult to provide a more detailed description or interpretation of the results.*

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 04

This is a medication with NDC code 68180-750-09 containing amlodipine besylate USP of 2.5mg per tablet. The medication should be dispensed in tight, light-resistant containers and stored at 20° to 25°C. The dosage and use instructions for this medication should be obtained from the accompanying prescribing information. The tablets are manufactured for Lupin Pharmaceuticals, Inc. in Baltimore. The medication comes in a bottle of 90 tablets and may only be used with a prescription.*

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 05

This text is a medicine label and provides dosage, usage, and storage instructions for Amlodipine Besylate tablets. It also lists the manufacturer's name, location, and code number.*

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 06

This is a medication with the National Drug Code (NDC) 68180-751-09 used for hypertension. Each tablet contains 5mg of amlodipine. It is available in a bottle containing 90 tablets, and it is indicated for prescription use only. The recommended dosage and usage information can be found in the provided prescribing information. The tablets should be dispensed in light-resistant containers and stored at a controlled room temperature of 20° to 25°C (68° to 77°F) to prevent exposure to light. The medication was produced by Lupin Pharmaceuticas in the USA and manufactured by Lupin Limited in India. No additional information is available.*

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 07

This text contains information about Amlodipine Besylate tablets, which are used to treat high blood pressure and chest pain (angina). The tablets come in a bottle with a tight, light-resistant cap and should be stored at room temperature. Each tablet contains 5mg of amlodipine besylate USP equivalent. The manufacturer is Lupin Pharmaceuticals, located in Baltimore, and the tablets are produced by Lupin Limited, in India. No dosage instructions or side effects are given in this text.*

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 08

This is a medication with the NDC code 68180-752-09, containing amlodipine besylate. Each tablet is equivalent to 10 mg of amlodipine. The medication should be stored in tight, light-resistant containers at room temperature (20° to 25°C / 68° to 77°F). Dispensing of the medication requires accompanying prescribing information. It is manufactured by Lupin Limited for Lupin Pharmaceuticals, Inc. in Baltimore, Maryland. The package contains 90 tablets and bears the code number MH/DRUGS/633.*

FDA Label Image

Afcca25d 0e19 4800 A55d 1714067a4400 09

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.