Product Images Levetiracetam

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Product Label Images

The following 11 images provide visual information about the product associated with Levetiracetam NDC 16571-789 by Rising Pharma Holdings, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Figure 1: Responder Rate (≥50% Reduction from Baseline) in Study 1 - levetiracetam fig1

Figure 1: Responder Rate (≥50% Reduction from Baseline) in Study 1 - levetiracetam fig1

The figure shows the Responder Rate with a 250% reduction from the baseline in Study 1. There is a statistically significant difference compared to the placebo. The rest of the text contains some percentages and medication names with unclear context.*

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 1000 mg (500 Tablets Bottle) - levetiracetam fig10

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 1000 mg (500 Tablets Bottle) - levetiracetam fig10

This is a description of Levetiracetam tablets USP, a medication used for seizures. Each film-coated tablet contains Levetiracetam USP 1000mg, and the usual dosage should be taken as per the package insert. It is recommended to store the tablets in a tight, light-resistant container with a child-resistant closure at a temperature between 20-25°C. The tablets are distributed by Rising Pharma Holdings, Inc. and were made in India. The text also includes a code and a printing/coding area.*

Figure 2: Responder Rate (≥50% Reduction from Baseline) in Study 2: Period A - levetiracetam fig2

Figure 2: Responder Rate (≥50% Reduction from Baseline) in Study 2: Period A - levetiracetam fig2

This is a graphic representation of the responder rate in a study conducted with three different groups of patients: those receiving a placebo, those taking 1000 mg/day of the medication Levetiracetam, and those taking 2000 mg/day of the same medication. The percentages represent the proportion of patients in each group who experienced a 250% reduction from their baseline symptoms. One of the groups taking 2000 mg/day showed a statistically significant improvement compared to the placebo group.*

Figure 3: Responder Rate (≥50% Reduction from Baseline) in Study 3 - levetiracetam fig3

Figure 3: Responder Rate (≥50% Reduction from Baseline) in Study 3 - levetiracetam fig3

This is a figure from a medical study (Study 3) showing the responder rate of patients who experienced a reduction of more than 50% from their baseline in the symptoms being treated. The responder rate was 45% for the placebo group (N=104) and 39.4% for the group receiving 3000mg per day of Levetiracetam (N=180). The figure also indicates that the Levetiracetam group had a statistically significant improvement compared to the placebo group.*

Figure 4: Responder Rate (≥ 50% Reduction from Baseline) in Study 4 - levetiracetam fig4

Figure 4: Responder Rate (≥ 50% Reduction from Baseline) in Study 4 - levetiracetam fig4

The text describes a figure named "Figure 4" that displays the responder rate in a study referred to as "Study 4". The graph shows that the responder rate was 44.6% and 45% for the Levetiracetam (N=101) group, respectively. For the placebo group (N=97), the responder rate was 19.6%. The figure suggests that the Levetiracetam group had a statistically significant higher responder rate compared to the placebo group.*

Figure 5: Responder Rate for All Patients Ages 1 Month to < 4 Years (≥ 50% Reduction from Baseline) in Study 5 - levetiracetam fig5

Figure 5: Responder Rate for All Patients Ages 1 Month to < 4 Years (≥ 50% Reduction from Baseline) in Study 5 - levetiracetam fig5

Figure 5 shows the Responder Rate for patients between 1 month and less than 4 years, with more than 50% reduction from the initial results, as recorded in Study 5. The percentage of Responder Rate is not available as the readings are inaccurate. However, Lovetracatam proved statistically significant compared to placebo in this study.*

Figure 6: Responder Rate (≥50% Reduction from Baseline) in PGTC Seizure Frequency per Week in Study 7 - levetiracetam fig6

Figure 6: Responder Rate (≥50% Reduction from Baseline) in PGTC Seizure Frequency per Week in Study 7 - levetiracetam fig6

This figure displays the responder rate in PGTC seizure frequency per week in Study 7. The graph shows the percentage of patients who had a 250% reduction from baseline in seizure frequency. The percentages for placebo and Levetiracetam (a medication) are shown on the y-axis, ranging from 0% to 100%. The x-axis shows the number of patients. The graph indicates that 72.2% of patients taking Levetiracetam had a 250% reduction in seizure frequency, compared to only 45.2% of patients taking placebo. The difference is statistically significant.*

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 250 mg (500 Tablets Bottle) - levetiracetam fig7

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 250 mg (500 Tablets Bottle) - levetiracetam fig7

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 500 mg (500 Tablets Bottle) - levetiracetam fig8

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 500 mg (500 Tablets Bottle) - levetiracetam fig8

Levetiracetam is a medication manufactured by Rising Pharma Holdings, Inc. Each film-coated tablet contains 500mg of Levetiracetam USP. Complete dosage recommendations can be found in the package insert. The drug should be dispensed in a tight, light-resistant container with a child-resistant closure. It should be stored at 20°C to 25°C (68°F to 77°F) with excursions permitted to 15°C to 30°C (59°F to 86°F). A medication guide is provided separately. Printed lines in the overprinting zone coding area are not to be printed.*

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 750 mg (500 Tablets Bottle) - levetiracetam fig9

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 750 mg (500 Tablets Bottle) - levetiracetam fig9

Chemical Structure - levetiracetam str

Chemical Structure - levetiracetam str

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.