منابع مشابه
A Validated Stability Indicating HPTLC Method for Determination of Cephalexin in Bulk and Pharmaceutical Formulation
A simple, specific, precise and stability-indicating high performance thin layer chromatographic method of analysis of Cephalexin, both as a bulk drug and in formulation was developed and validated. The method employed TLC (Thin Layer Chromatography) aluminum plates pre-coated with silica gel 60 F254 as the stationary phase. The solvent system consisted of Ethyl Acetate : Methanol : Ammonia (6:...
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Packaging of pharmaceuticals is a critical process. It is an economical means of providing protection, presentation, information, identiÞ cation, containment, administration, shelf-life and convenience for a product during carriage, storage, display and ultimate total use, paying due attention to any legal and environmental factors1. Plastics are a wide group of solid composite materials, which...
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Cephalexin for Oral Suspension, USP, is a pink colored powder forming pink colored suspension on constitution. After mixing, each 5 mL of cephalexin for oral suspension, will contain cephalexin USP equivalent to 125 mg (360 μmol) or 250 mg (720 μmol) of anhydrous cephalexin. The suspension also contains the following inactive ingredients: colloidal silicon dioxide, FD&C Red No. 40, sodium benzo...
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Oseltamivir (Tamiflu) is widely prescribed to treat and prevent influenza virus A, influenza virus B, and H1N1 Flu. It is manufactured by Roche in 75-mg capsules. The need for other administration options for patients who cannot take capsules and cannot use suspending agents which contain alcohol, sorbitol, or preservatives has led to the compounding of oseltamivir into three suspending vehicle...
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ژورنال
عنوان ژورنال: Japanese Journal of Hospital Pharmacy
سال: 1980
ISSN: 2185-9477,0389-9098
DOI: 10.5649/jjphcs1975.6.103