What does the US Pharmacopeia do?
What does the US Pharmacopeia do?
The United States Pharmacopeial Convention (USP) is a nonprofit scientific organization founded in 1820 in Washington, D.C., that develops and disseminates public compendial quality standards for medicines and other articles (Bylaws, Articles II, and VII).
What is difference between USP and IP?
I.P., the abbreviation of ‘Indian Pharmacopoeia’ is familiar to the consumers in the Indian sub-continent as a mandatory drug name suffix. suffix for British Pharmacopoeia and the U.S.P. suffix for the United States Pharmacopeia.
What is in a pharmacopeia?
A pharmacopoeia is a legally binding collection of standards and quality specifications for medicines used in a country or region. A pharmacopoeia also covers pharma- ceutical starting materials, excipients, intermediates and finished pharma- ceutical products (FPPs).
Why use United States Pharmacopeia as a reference?
Developing documentary standards and Reference Standards is the core of what we do at USP. These standards help to assess the quality, strength, identity, and purity of chemical medicines, biologics, food chemicals and ingredients, dietary supplements, among other items.
Why does the US have Pharmacopeia?
United States Pharmacopeia: Abbreviated USP. A publication, established in 1820, that contains legally recognized standards of identity, strength, quality, purity, packaging, and labeling for drug substances, dosage forms, and other therapeutic products, including nutritionals and dietary supplements.
Who published Indian Pharmacopoeia?
the Indian Pharmacopoeia Commission
It is published by the Indian Pharmacopoeia Commission (IPC) on behalf of the Ministry of Health & Family Welfare, Government of India, in fulfillment of the requirements of the Drugs and Cosmetics Act, 1940 and the Rules thereunder.
How do you cite US Pharmacopeia?
Citation Data
- MLA. The United States Pharmacopeia. The National Formulary.
- APA. The United States pharmacopeia. The National formulary. (
- Chicago. “The United States Pharmacopeia. The National Formulary.” Rockville, Md. :United States Pharmacopeial Convention, Inc., 1979.
What is the US Pharmacopeia National Formulary?
The United States Pharmacopeia – National Formulary (USP-NF) includes over 5000 quality standards for medicines, both chemical and biologic; active pharmaceutical ingredients (APIs); and excipients (inactive ingredients). USP is an official quality standard for medicines marketed in the US.
What is pharmacopoeia derived from?
Etymology. The term derives from Ancient Greek: φαρμακοποιία pharmakopoiia “making of (healing) medicine, drug-making”, a compound of φάρμακον pharmakon “healing medicine, drug, poison”, the verb ποιεῖν poiein “to make” and the abstract noun suffix -ία -ia.
What is Pharmacopeia quality?
The role of a modern pharmacopoeia is to furnish quality specifications for active pharmaceutical ingredients (APIs), FPPs and general requirements, e.g. for dosage forms. The existence of such specifications and requirements is necessary for the proper functioning or regulatory control of medicines.
