USP Type I borosilicate glass is the least reactive glass available for containers. It can be used for all applications and is most commonly used to package water for injection, UN-buffered products, chemicals, sensitive lab samples, and samples requiring sterilization. All lab glass apparatus is generally Type I borosilicate glass. Examples of Type I borosilicate glass include Corning® Pyrex® 7740 and Wheaton 180, 200, and 400. Though Corning® Vycor® 7913 is not classified as a Type I glass, it does meet or exceed USP Type I requirements.
In most cases Type I glass is used to package products which are alkaline or will become alkaline prior to their expiration date. Care must be taken in selecting containers for applications where the pH is very low or very high, as even Type I glass can be subject to attack under certain conditions. Although Type I borosilicate has the least pH shift of any glass, there still may be some sensitivity with certain packaged products.
Surface treatment is not usually required, however it will further enhance the desirable characteristics of an already superior container. This surface enhancement may become especially important for small containers because of the high ratio of container surface area to the volume of the container contents.
USP Type II de-alkalized soda-lime glass has higher levels of sodium hydroxide and calcium oxide. It is less resistant to leaching than Type I but more resistant than Type III. It can be used for products that remain below pH 7 for their shelf life.
USP Type III soda-lime glass is acceptable in packaging some dry powders which are subsequently dissolved to make solutions or buffers. It is also suitable for packaging liquid formulations that prove to be insensitive to alkali. Type III glass should not be used for products that are to be autoclaved, but can be used in dry heat sterilization. Examples of Type III soda lime glass include Wheaton 800 and 900.
USP Type NP soda-lime glass is a general purpose glass and is used for non-parenteral applications where chemical durability and heat shock are not factors. These containers are frequently used for capsules, tablets and topical products. Examples of Type NP glass include Wheaton 810 and 910.
Yes, USP mineral oil is considered food grade as it meets the standards set by the United States Pharmacopeia (USP) for purity and safety for use in food and pharmaceutical applications. It is often used in food processing and preparation, as well as in the manufacture of medicines and personal care products.
The defoaming test as per the United States Pharmacopeia (USP) evaluates the efficacy of a defoaming agent in reducing or inhibiting foam formation in pharmaceutical formulations. This test typically involves adding the defoaming agent to a specified volume of a foaming solution and measuring the time taken for foam to dissipate or the volume of foam produced. The results help ensure product stability and performance, particularly for liquid formulations like emulsions or suspensions. Compliance with USP guidelines ensures that the defoaming agent's effectiveness meets required pharmaceutical standards.
USP method 905 "Uniformity of Dosage Units" describes how to calculate the weight variation for your dosage forms. If you need a copy of method simply drop me an email at waqassial@hotmail.com Regards
USP is "United States Pharmacopeia". FCC is probably "food chemicals codex". They both mean that the chemical in question conforms to the purity standards of the document specified. What that means PRECISELY you'd have to look up in said document, but in both cases it means roughly "this compound is pure enough to use in making drugs (USP) or foods (FCC)." On the purity scale, USP/FCC is usually somewhat less than spectroscopy grade, but better than lab grade or reagent grade.
USP grade refers to a set of standards established by the United States Pharmacopeia for the purity, quality, strength, and consistency of drugs, food ingredients, and dietary supplements. Substances labeled as USP grade meet the specific criteria outlined in the USP-NF monographs.
FCC (Food Chemicals Codex) grade and USP (United States Pharmacopeia) grade are two different standards for purity and quality. While USP is primarily focused on pharmaceutical products, FCC is specific to ingredients used in food and beverages. Although USP has acquired the FCC standards, they still remain distinct in their applications and requirements.
Yes, USP mineral oil is considered food grade as it meets the standards set by the United States Pharmacopeia (USP) for purity and safety for use in food and pharmaceutical applications. It is often used in food processing and preparation, as well as in the manufacture of medicines and personal care products.
The key differences between USP 42 and NF 37 are the standards they cover. USP 42 focuses on pharmaceuticals and related products, while NF 37 covers excipients and other non-pharmaceutical ingredients. Additionally, USP 42 includes monographs for drug substances and dosage forms, while NF 37 includes monographs for non-drug substances.
USP 797 has a large effect on pharmacies. A good source of information on usp 797 is www.usp797.org. This site has numerous usp 797 articles and a section on commonly asked questions and answers about usp 797. USP 797 has an enormous effect on pharmacies that compound sterile products. USP 797 is a far-reaching regulation that governs a wide range of pharmacy policies and procedures. It is designed both to cut down on infections transmitted to patients through pharmaceutical products and to better protect staff working in pharmacies in the course of their exposure to pharmaceuticals. Issued by U.S. Pharmacopoeia (USP), the regulation governs any pharmacy that prepares "compounded sterile preparations" (CSPs). Many pharmacies fit this description. Moreover, many large hospitals have several pharmacies--a main one and several satellite pharmacies--that will be affected. An excellent source for information about usp 797 is the website: www.usp797.org. What you will find on USP797.org : USP 797 regulations, USP 797 vendors, USP 797 articles, and USP 797 software.
Yes, Pantoprazole sodium is included as an official monograph in the United States Pharmacopeia and National Formulary (USP-NF) 30. This monograph provides standards for the identity, quality, purity, and strength of Pantoprazole sodium for pharmaceutical use.
BP - British Pharmacopoeia and USP - United States Pharmacopeia.In the world there are various pharmacopeias which are guidelines for the Pharmaceutical Industry for manufacture and testing of drugs. BP and USP are two of approximately 30 country or region run pharmacopeias. In the BP and USP there are specific tests which must be followed to be labeled BP or USP and depend on which drug (aspirin, acetominophen, etc) is being tested. In the US, it is a legal requirement that all drugs meet or exceed the USP. In various other places the laws may not be as strict to where any pharmacopeia may be used (British, Canadian, Japanese, US, European etc).
USP method 905 "Uniformity of Dosage Units" describes how to calculate the weight variation for your dosage forms. If you need a copy of method simply drop me an email at waqassial@hotmail.com Regards
What are the advantage of the USP?
Mineral oil USP is commonly used in the pharmaceutical, cosmetic, and food industries. In pharmaceuticals, it is used as a lubricant in tablets and capsules. In cosmetics, it is used in skincare products as a moisturizer and emollient. In the food industry, it is used as a lubricant for machinery and as a release agent in food processing.
what is usp of allahabad bank
Petrolatum USP, also known as petroleum jelly or mineral jelly, is a semi-solid mixture of hydrocarbons derived from petroleum. It is designated as "USP" (United States Pharmacopeia) to indicate that it meets specific quality standards for pharmaceutical and medical use. Commonly used as a topical ointment, it acts as a moisturizer and barrier to protect the skin from moisture loss and external irritants. Its applications extend to personal care products, cosmetics, and various medicinal formulations.
USP is "United States Pharmacopeia". FCC is probably "food chemicals codex". They both mean that the chemical in question conforms to the purity standards of the document specified. What that means PRECISELY you'd have to look up in said document, but in both cases it means roughly "this compound is pure enough to use in making drugs (USP) or foods (FCC)." On the purity scale, USP/FCC is usually somewhat less than spectroscopy grade, but better than lab grade or reagent grade.