All Posts - Pharma Egg

May312023 by KBS.No Comments

Sumatriptan as Succinate 85mg and Naproxen Sodium 500mg Tablet Testing Procedure By UV and HPLC Method

Testing Methods, Product, Quality Control, SOPs

To determine Sumatriptan succinate (85mg) and Naproxen sodium (500mg) in a tablet formulation, both UV spectrophotometry and HPLC methods can be utilized. Sumatriptan as Succinate 85mg and Naproxen Sodium 500mg Tablet Testing Procedure By UV and HPLC Method Here's an outline of the testing procedures for each method: PURPOSE To describe the procedure for analysis at the in-process and finished stage of Sumatriptan as Succinate 85mg per Tablet and Naproxen Sodium 500mg per Tablet Tablet. SCOPE This SAP gives a detailed outline for the finished product analysis of Sumatriptan as Succinate 85mg per Tablet and Naproxen Sodium 500mg per Tablet and will cover In process testing activities on a physical, chemical & instrumental basis. RESPONSIBILITY QC Analyst is responsible for physica...

May312023 by KBS.No Comments

Determination of Nimesulide in Pharmaceutical Dosage Forms by UV Spectrophotometry and HPLC Method

Testing Methods, Product, Quality Control, SOPs

Both UV spectrophotometry and HPLC methods provide reliable and accurate results for the determination of Nimesulide in pharmaceutical dosage forms. The choice of method depends on factors such as the required sensitivity, specificity, and available equipment. Determination of Nimesulide in Pharmaceutical Dosage Forms by UV Spectrophotometry and HPLC Method is recommended to follow official pharmacopoeial methods or validated analytical procedures for accurate and precise analysis. PURPOSE: To describe the procedure for analysis at the in-process and finished stage of the Nimesulide Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of the Nimesulide Tablet and will cover In process testing activities on a physical, chemical & instrumental basis. RE...

May252023 by KBS.No Comments

Hplc and UV Testing Method of Montelukast Sodium in Tablet

Testing Methods, Product, Quality Control, SOPs

It is important to note that the specifics of the assay method, including the instrumentation, chromatographic conditions (for HPLC), wavelength selection (for UV spectrophotometry), and sample preparation steps, may vary depending on the official compendial method, published literature, or specific requirements of your laboratory. Hplc and UV Testing Method of Montelukast Sodium in Tablet It is recommended to consult relevant references or validated methods for detailed experimental conditions. PURPOSE: To describe the procedure for analysis at the in-process and finished stage of Montelukast Sodium Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of the Montelukast Sodium Tablet and will cover In process testing activities on physical, chemical &...

May242023 by KBS.No Comments

Assay Testing Procedure for Topiramate Tablet

Testing Methods, Product, Quality Control, SOPs

This is a general overview of the assay testing procedure for Topiramate tablets. The specific details and requirements may vary depending on the official pharmacopeial methods or the requirements of the testing laboratory. It is important to consult the relevant official compendium or laboratory procedures for precise instructions and guidelines. The assay testing procedure for Topiramate tablets involves determining the quantity or concentration of the active ingredient, topiramate, in the tablet formulation. Here is a general outline of the procedure: PURPOSE: To describe the procedure for Assay Testing Procedure for Topiramate Tablet analysis at the in-process and finished stage of Topiramate Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of Top...

Apr32023 by KBS.No Comments

SOP for Finished Product Analysis of Olanzapine Tablet By UV and HPLC Method

Testing Methods, Product, SOPs

These tests are typically performed in accordance with the guidelines set forth by the United States Pharmacopeia (USP) or other regulatory agencies. The testing procedure for Olanzapine tablets typically includes the following steps By SOP for Finished Product Analysis of Olanzapine Tablet By UV and HPLC Method: Identification: The tablets are identified by their physical characteristics, including their size, shape, color, and markings. Assay: The assay determines the quantity of active ingredient (olanzapine) in the tablet. This is done using a validated analytical method such as high-performance liquid chromatography (HPLC). Dissolution: The dissolution test determines how quickly the tablet dissolves and releases the active ingredient. This is important because the rate of di...

Mar272023 by KBS.19 Comments

SOP for Pirfenidone 267 mg tablet Tablet Testing with UV Method

Testing Methods, Product, Quality Control, SOPs

Pirfenidone 267 mg Tablet Testing with UV Method is a common method used to determine the presence and concentration of Pirfenidone in the tablet. The UV method relies on the absorption of light by the active ingredient, Pirfenidone, at a specific wavelength. SOP for Pirfenidone 267 mg tablet Tablet Testing with UV Method testing is done as per the SOP for Pirfenidone 267 mg Tablet Testing with UV Method. In addition to the UV method, other tests like physical tests (appearance, weight variation, disintegration, and hardness), and chemical tests (pH, assay, and impurities) are also performed to ensure the quality of the tablets. Overall, Pirfenidone 267 mg Tablet Testing with UV Method is an important part of quality control in the pharmaceutical industry to ensure that the tablets a...

Mar272023 by KBS.No Comments

SOP for Pantoprazole Sodium 40mg Tablet Testing HPLC and UV Method

Testing Methods, Product, Quality Control, SOPs

Pantoprazole Sodium 40mg Tablet Testing is performed to check the quality and potency of the tablets. The testing is done using various methods such as HPLC, UV, and dissolution testing. HPLC method is used to determine the amount of Pantoprazole Sodium in the tablet. The SOP for Pantoprazole Sodium 40mg Tablet Testing HPLC and UV Method is used to identify the presence of Pantoprazole Sodium in the tablet. Dissolution testing is used to determine the rate at which the active ingredient is released from the tablet. In addition to these tests, other tests like physical tests (appearance, weight variation, disintegration, and hardness), and chemical tests (pH, assay, and impurities) are also performed to ensure the quality of the tablets. Overall, Pantoprazole Sodium 40m...

Mar252023 by KBS.No Comments

Rabeprazole sodium Tablet Complete Testing Procedure (SOP)

Testing Methods, Product, SOPs

Both UV and HPLC methods are commonly used to test Rabeprazole sodium tablets for their active ingredient content. These methods are reliable, accurate, and precise, and are widely accepted by regulatory authorities. Rabeprazole sodium Tablet Complete Testing Procedure (SOP) PURPOSE: To describe the procedure for analysis at in-process and finished stage of Rabeprazole sodium 20mg Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of Rabeprazole sodium 20 mg Tablets and will cover In process testing activities on a physical, chemical & instrumental basis. RESPONSIBILITY: QC Analyst is responsible for physical / chemical testing and preparing standard analytical procedure. It is the responsibility of QC Manager to assist and ensure Testing Procedur...

Mar252023 by KBS.No Comments

SOP for Ranolazine XR Tablet Testing HPLC and UV Method

Testing Methods, Product, SOPs

In terms of testing, Ranolazine XR 500mg Tablet has undergone various clinical trials to establish its safety and efficacy. SOP for Ranolazine XR Tablet Testing HPLC and UV Method clinical trials have been conducted on a large number of patients with chronic angina, and the results have been published in peer-reviewed medical journals. The clinical trials have demonstrated that Ranolazine XR 500mg Tablet is effective in reducing the frequency of angina episodes, improving exercise tolerance, and improving the quality of life in patients with chronic angina. The medication has also been found to be safe, with no significant side effects observed in most patients. PURPOSE: To describe the procedure for analysis at in-process and finished stage of Ranolazine XR 500mgTablet. SCOPE: This...

Mar252023 by KBS.No Comments

Rivaroxaban Tablet Testing HPLC and UV Method

Testing Methods, Product, SOPs

In terms of testing, the in-process stage of Rivaroxaban tablet testing would typically involve quality control measures to ensure that the tablets are being produced according to the intended specifications. This could include tests to check the tablet's weight, thickness, hardness, and disintegration time. Rivaroxaban Tablet Testing HPLC and UV Method may also undergo testing for purity and content uniformity. The finished stage of testing involves a series of quality control tests to ensure that the tablets meet the required standards for safety, efficacy, and quality before they are released for distribution. These tests could include identification tests, assay tests, dissolution tests, and impurity tests. The tablets may also undergo stability testing to ensure that they remain ef...