Losartan Potassium Tablet, Film Coated
Product Images NDC 33342-045

14 FDA label images from Macleods Pharmaceuticals Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 33342-045). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals 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

Losartan Figure 10

Losartan Figure 10
Label for Losartan Potassium Tablets, USP 50 mg by Macleods Pharmaceuticals Ltd. The film-coated oral tablets package contains 1000 tablets. It includes storage instructions, dosage directions, and labeling for pharmacist dispensing. Manufactured by Macleods Pharmaceuticals Ltd. in India and labeled for Macleods Pharma USA, Inc.*
FDA Label Image

Losartan Figure 13

Losartan Figure 13
The label for Losartan Potassium Tablets, USP 100 mg, film coated, by Macleods Pharmaceuticals Limited and Macleods Pharma USA, Inc. It indicates a prescription oral tablet with a package size of 1000 tablets. Storage instructions specify 20° to 25°C with permitted excursions. The label also includes manufacturer detail, lot and expiration date fields, and a note to dispense patient information leaflets with the pack.*
FDA Label Image

Losartan Figure 5

Losartan Figure 5
Packaging label for Losartan Potassium Tablets, USP 25 mg, film coated. The label indicates a 30-tablet count and is labeled by Macleods Pharmaceuticals Limited. The label includes storage instructions, dosage reference, and manufacturer details for Macleods Pharma USA, Inc. and Macleods Pharmaceuticals Ltd.*
FDA Label Image

Losartan Figure 7

Losartan Figure 7
Label for Losartan Potassium Tablets USP 25 mg, oral film-coated tablets. The label indicates the product is supplied in a quantity of 1000 tablets and is manufactured by Macleods Pharmaceuticals Ltd., India, for Macleods Pharma USA, Inc. The label includes storage instructions and states the tablet strength as 25 mg of losartan potassium.*
FDA Label Image

Losartan Figure No 11

Losartan Figure No 11
Label for Losartan Potassium Tablets USP 100 mg, film-coated oral tablets. The package contains 30 tablets. Manufactured by Macleods Pharmaceuticals Ltd., India, and labeled for Macleods Pharma USA, Inc., Plainsboro, NJ. The label includes storage conditions, dosage reference, and pharmacy dispensing instructions, along with barcodes and batch/expiration placeholders.*
FDA Label Image

Losartan Figure No 12

Losartan Figure No 12
Losartan Potassium Tablets, USP 100 mg film-coated tablets packaging label from Macleods Pharmaceuticals Limited. The label includes storage instructions, prescription information, and states the product is manufactured for Macleods Pharma USA, Inc. The package contains 90 tablets and is labeled for oral use.*
FDA Label Image

Losartan Figure No 3

Losartan Figure No 3
A forest plot chart comparing Losartan potassium and Atenolol event rates for primary composite outcomes and stroke (fatal/non-fatal) across patient subgroups by age, gender, race, ISH, diabetes, and history of cardiovascular disease. The chart shows hazard ratios with 95% confidence intervals, numbers of patients, and event rates for each group.*
FDA Label Image

Losartan Figure No 6

Losartan Figure No 6
Losartan Potassium Tablets USP 25 mg film-coated, 90 count, manufactured for Macleods Pharma USA, Inc. The label displays medication storage instructions and manufacturer details: Macleods Pharmaceuticals Ltd., Baddi, Himachal Pradesh, India. The NDC code is 33342-044-10. It includes dispensing notes for the pharmacist.*
FDA Label Image

Losartan Figure No 8

Losartan Figure No 8
Losartan Potassium Tablets USP 50 mg film-coated tablets label by Macleods Pharmaceuticals Limited. The label indicates a 30-tablet bottle for oral use, manufactured by Macleods Pharmaceuticals Ltd. in India and for Macleods Pharma USA, Inc. The label includes storage instructions, barcode, and prescription-only status.*
FDA Label Image

Losartan Figure No 9

Losartan Figure No 9
Losartan Potassium Tablets USP 50 mg film-coated tablet label by Macleods Pharmaceuticals Limited. The label indicates 90 tablets per container, mentions prescription use only, and provides storage instructions. Manufactured for Macleods Pharma USA, Inc., Plainsboro, NJ, and manufactured by Macleods Pharmaceuticals Ltd., India.*
FDA Label Image

Losartan Figure1

Losartan Figure1
A line graph comparing the percentage of patients with a primary endpoint over 66 study months for Losartan Potassium and Atenolol. The graph shows time on the x-axis (Study Month) and percentage on the y-axis (% patients with primary endpoint), illustrating adjusted risk reduction for Losartan Potassium versus Atenolol.*
FDA Label Image

Losartan Figure2

Losartan Figure2
A line graph comparing the percentage of patients with fatal or mortal stroke over study months between Atenolol and Losartan Potassium groups. The graph shows a lower incidence in the Losartan Potassium group, with an adjusted risk reduction of 25% and p-value of 0.001, demonstrating comparative outcomes over time.*
FDA Label Image

Losartan Figure4

Losartan Figure4
A line graph comparing the percentage of patients with an event over 48 months for Losartan potassium versus placebo. The graph indicates a risk reduction of 16.1% with Losartan potassium and includes statistical significance (p=0.022). The x-axis represents time in months, and the y-axis represents the percentage of patients with an event.*
FDA Label Image

Losartan Structure

Losartan Structure
Chemical structure of losartan potassium, showing its molecular arrangement including a chlorinated biphenyl group, tetrazole ring, hydroxymethyl group, and potassium ion.*

* 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.