摘要:
The present invention relates to an extended release composition comprising milnacipran or its pharmaceutically acceptable salts for oral administration, and process for their preparation.
摘要:
The present invention relates to orally disintegrating compositions comprising angiotensin II receptor antagonists. It also relates to orally disintegrating compositions comprising combination of angiotensin II receptor antagonists and other antihypertensive drugs. It further relates to processes for preparing such compositions. It also relates to method of treating hypertension and congestive heart failure using the compositions of the present invention.
摘要:
The field of the invention relates to stable dosage forms comprising spiro or dispiro 1,2,4-trioxolane antimalarials, or their pharmaceutically acceptable salts, prodrugs and analogues, and processes for their preparation. The water content of the dosage form is not more than 6.5% w/w.
摘要:
The present invention relates to an orally administered pharmaceutical composition that is a combination of two or more antidiabetic agents in which one of the antidiabetic agents is present in an extended release form and the other antidiabetic agent is present in an immediate release form.
摘要:
The present invention relates to a modified release composition comprising milnacipran or its pharmaceutically acceptable salts, and process for their preparation.
摘要:
The present invention relates to a pharmaceutical composition comprising low- dose metaxalone and one or more pharmaceutically acceptable polymer, as well as methods of preparing them.
摘要:
The present invention relates to a new process for preparing an oral pharmaceutical composition comprising fenofibrate alone or in combination with at least one other antilipidemic agent in a single dosage form that can be conveniently administered once or twice in a day.
摘要:
The present invention relates to co-precipitated amorphous cefditoren pivoxil dosage forms and processes for their preparation. The process includes preparing a solution of crystalline cefditoren pivoxil in one or more solvents; dispersing one or more water insoluble carriers in the solution; and removing the solvent. The amorphous cefditoren pivoxil and one or more water insoluble carriers are co-precipitated from the solution.
摘要:
The invention relates to a delayed release pharmaceutical composition of mesalamine comprising: a) granules comprising mesalamine or pharmaceutically acceptable salts thereof and a hydrophilic polymer; b) extragranular excipients; wherein the pharmaceutical composition is further coated with a single layer of polymer.
摘要:
The present invention relates to a process for preparing a carbapenem antibiotic composition, Formula (II). The present invention further relates to a carbapenem antibiotic composition substantially free of degradation impurities. The present invention further relates to a polymorphic form of ertapenem monosodium designated as Form D and its preparation.