FAQs of Clopidogrel Bisulfate BP-USP:
Q: How should Clopidogrel Bisulfate BP-USP be stored to maintain its quality?
A: Clopidogrel Bisulfate BP-USP should be kept in a dry place to prevent moisture absorption, which helps maintain its stability and prolongs its shelf life up to four years.
Q: What is the primary usage of Clopidogrel Bisulfate BP-USP powder?
A: This product serves as a pharmaceutical intermediate, mainly used in the synthesis of antiplatelet agents such as Clopidogrel, which helps prevent blood clots.
Q: When is Clopidogrel Bisulfate BP-USP typically used during the pharmaceutical manufacturing process?
A: Clopidogrel Bisulfate BP-USP is introduced during the intermediate stages of active pharmaceutical ingredient synthesis before formulating the final medication.
Q: Where does Clopidogrel Bisulfate BP-USP exhibit optimal solubility?
A: It is freely soluble in highly acidic environments (at pH 1) but remains practically insoluble at neutral pH, making it suitable for specific pharmaceutical formulations.
Q: What process ensures the consistent free-flowing appearance of Clopidogrel Bisulfate BP-USP?
A: Careful manufacturing and stringent drying protocols result in the powders white to off-white color and free-flowing texture, which simplifies handling during production.
Q: What are the main benefits of using Clopidogrel Bisulfate BP-USP for manufacturers?
A: Manufacturers benefit from its high purity, long shelf life, easy handling, and compliance with BP and USP standards, ensuring consistent and reliable pharmaceutical outputs.