The present invention discloses an Orlistat composition which has an averages particle size of pellets of not less than or equal to 2mm and is devoid of microcrystalline cellulose. The invention further discloses a process for manufacturing thereof.
The present invention discloses a pharmaceutical formulation for treatment of benzimidazole induced hypomagnesaemia. The formulation of the invention contains a therapeutically effective amount of benzimidazole and therapeutically effective amount of dietary Magnesium source. The invention further relates to a proce...
The present invention discloses a novel stable formulation for D-enantiomer of
rabeprazole containing a primary amine as stabilizing agent and process for manufacturing thereof.
Novel acid resistant pharmaceutical composition of Duloxetine comprises
Hydroxypropyl methyl Cellulose Trimellitate (HPMCT) as an enteric polymer and a process for manufacturing thereof.
The present invention relates to a novel Cilostazol composition. More particularly, the invention relates to a novel sustained release formulation of Cilostazol, which is essentially devoid of any release controlling agent, and the process for formulation thereof.
Galantamine extended release pellets / particles /beads and the like and the process for preparing the formulation wherein the release is extended by the Dual retard technique imparted by the Galantamine Hydrobromide - Glyceryl behenate Complex obtained by the hot melt process and further by the extended release coa...
The invention relates to a method of preparation of an instant release oral solid dosage form of an insoluble 5α-reductase inhibitor and pharmaceutical preparations containing thereof particularly in the form of drug coated non pareil seeds or pellets or beads comprising the active.
Aspects of the present disclosure relate to controlled release formulation comprising at least one substituted benzimidazole derivative, which in operation can provide effective plasma concentration thereof to a subject in need of a treatment over an extended period of time. An aspect of the present disclosure provi...
ABSTRACT
A METHOD FOR THE PREPARATION OF PHARMACEUTICAL COMPOSITION OF LEVOTHYROXINE ORAL SOLUTION
The present invention relates to a method for the preparation of pharmaceutical composition of levothyroxine oral solution. The present invention is in particular about the method of preparing stable pharmaceutic...
Controlled release pharmaceutical composition of mirabegron
The present invention relates to a controlled release pharmaceutical composition of mirabegron comprising mirabegron or a pharmaceutically acceptable salt thereof and a non hydrogel-forming excipient selected from glycerol dibehenate, ethyl cellulose, ce...
Pharmaceutical composition of docusate and process for preparation thereof
The present invention relates to a pharmaceutical composition of docusate and process for its preparation. The pharmaceutical composition optionally further comprises sennosides. The pharmaceutical composition of the present invention is pre...
Extended release pharmaceutical composition of mirabegron
The present invention relates to an extended release pharmaceutical composition of mirabegron comprising mirabegron or a pharmaceutically acceptable salt thereof, polyethylene glycol having an average molecular weight of 1,800 to 9,000, polyethylene oxide ha...