Losartan Potassium Tablet, Film Coated
Product Images NDC 70518-0245

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 70518-0245). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Losartan Potassium 50mg 70518 0245 01)

Mm2 (Losartan Potassium 50mg 70518 0245 01)
This is a prescription medicine with the name Losartan Potassium. Each package contains 90 tablets with a strength of 50mg each. The manufacturer of the medicine is Aurohindo Pharma Ltd. It is recommended to keep this medication away from children. The directions for use can be found in the package insert. The medication should be stored at a temperature between 20-25°C (68-77°F) with excursions at 15-30°C (59-86°F). It was packaged by RemedyRepack Inc. located in Indiana, PA.*
FDA Label Image

Losartan Potassium 50mg 70518 0245 02

Losartan Potassium 50mg 70518 0245 02
Losartan Potassium is a tablet of 50 mg strength, available in a pack size of 60, manufactured by Aurohindo Pharma Ltd. The prescription drug is packaged by RemedyRepack Inc. The recommended storage temperature for the tablet is between 20-25°C (83-77°F), excursion permitted up to 15-30°C (53-86°F), as per USP guidelines. The package insert should be referred to for directions for use. The drug must be kept out of children's reach. The NDC number for RX-only Losartan Potassium 50 mg tablet is 70518-0245-02, and the Source NDC is 65862-0202-99.*
FDA Label Image

Remedy Label

Remedy Label
Losartan Potassium is a drug available in the form of a tablet with a strength of 50mg, packed by RemedyRepack INC. The package contains 30 tablets and the directions for use are provided in the package insert. The drug should be stored at a temperature between 20-25°C (53-86°F), and it is for Rx only. The manufacturer is Aurohindo Pharma Ltd., located in Nagar, India. The NDC # is 70518-0245-00, and it should be kept out of the reach of children. The other mentioned numbers are not available for interpretation.*
FDA Label Image

Figure1 (Losartan Fig1)

FDA Label Image

Figure2 (Losartan Fig2)

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Figure 3 (Losartan Fig3)

Figure 3 (Losartan Fig3)
The text provided is a table showing the breakdown of primary endpoint events within demographic subgroups. The subgroups are categorized by age, gender, race, and a few other factors. The table is difficult to read due to errors in the and missing information.*
FDA Label Image

Figure-4 (Losartan Fig4)

Figure-4 (Losartan Fig4)
This is a table showing the percentage of patients with an event related to the use of Losttan Potassium compared to a placebo. The table indicates that 60% of patients with event occurred with Losttan Potassium and 40% with placebo. The risk reduction is mentioned as 16.1% with p-value equal to 0.022. It seems that Losttan Potassium was being tested for its effectiveness in reducing the occurrence of the event.*
FDA Label Image

Chemical Structure (Losartan Str)

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