Brompheniramine Maleate USP Powder for Compounding Medications (API) (Rx)
(Note: We don’t Fill Personal Prescriptions)
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Brompheniramine Maleate USP Powder for Compounding Medications (API) is used to formulate antihistamine medications for the relief of allergy symptoms such as sneezing, runny nose, itchy eyes, and skin rashes. It works by blocking histamine receptors, reducing the effects of histamine in the body. Compounding pharmacists can tailor doses and formulations to meet specific patient needs, providing effective treatment for allergies and allergic reactions, and enhancing patient comfort by minimizing side effects and ensuring optimal therapeutic outcomes.
Brompheniramine maleate USP powder for compounding medications is a pharmaceutical active ingredient (API) used in the preparation of various prescription and over-the-counter medications for the treatment of allergic reactions, such as hives, runny nose, and itchy/watery eyes. It belongs to a class of drugs called antihistamines, which work by blocking the effects of histamine, a substance that is responsible for causing allergy symptoms. Brompheniramine maleate is available in powder form and must be compounded with other ingredients to produce a specific dosage form, such as tablets, capsules, or topical creams. Compounding pharmacies use brompheniramine maleate USP powder to customize medications according to a patient's unique needs, such as adjusting the strength or form of the medication to better suit the patient's condition and preferences.
Brompheniramine Maleate USP Powder is an antihistamine medication used to treat allergic reactions, including hay fever, hives, and seasonal allergies. It can also be used to relieve symptoms of the common cold and help with symptoms such as runny nose, sneezing, and watery eyes.
Brompheniramine Maleate, USP is an antihistamine used to alleviate symptoms of the common cold and allergic rhinitis. All Spectrum Chemical USP grade products are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.