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Carnipure™ crystalline | Carnipure™ tartrate |
100% pure L-Carnitine | Stable salt containing approximately 68% L-Carnitine, 32% natural L-tartaric acid |
White, crystalline powder | White, crystalline powder |
Highly water soluble, forms colorless solutions | Highly water soluble, forms colorless solutions |
Odorless | Odorless, pleasant fruity flavor |
Heat stable up to 120°C | Heat stable up to 120°C |
Hygroscopic – especially suitable for liquid applications | Non-hygroscopic – suitable for all solid and liquid applications |
Generally Recognized As Safe (GRAS) | Generally Recognized As Safe (GRAS) |
Excellent safety profile – LD50 could not be determined | Excellent safety profile – LD50 could not be determined |
Meets specifications of Food Chemicals Codex (F.C.C.) and United States Pharmacopoeia (U.S.P.) |
L-Carnitine and L-Tartaric acid used to produce L- Carnitine L-Tartrate meet specifications of F.C.C. and U.S.P. |
U.S. patent 5,073,376 and other international patents | |
Kosher, OU certified | Kosher, OU certified |
Free of animal products | Free of animal products |
Free of genetically modified organisms (GMOs) | Free of genetically modified organisms (GMOs) |
Product name | Pharmacopoeia | Specification |
PURAC® PF | USP, JP, EP | L (+) Lactic Acid pharma grade |
PURASAL® S/PF 50% | USP, EP, JPC | sodium–S–lactate pharma grade 50% |
PURASAL® S/PF 60% | USP, EP, JPC | sodium–S–lactate pharma grade 60% |
PURACAL® PP/USP | USP, EP | calcium lactate pharma grade |
PURACAL® DC | USP, EP | calcium lactate for direct compressible use |
PURACAL® XPRESS | calcium lactate gluconate pharma grade | |
GLUCONAL® CAM-P-IN-EP | EP | calcium gluconate monohydrate pharma grade for injectable applications |
GLUCONAL® CAM-P-IN | USP | calcium gluconate monohydrate pharma grade for injectable applications |
GLUCONAL® CAM-P-OR | USP, EP | calcium gluconate monohydrate pharma grade for oral applications |
GLUCONAL® CADS | USP | calcium D-saccharate |
GLUCONAL® FE-Pharma | USP, EP | ferrous gluconate pharma grade |
GLUCONAL® MG | USP | magnesium gluconate |
GLUCONAL® K | USP | potassium gluconate |
GLUCONAL® ZN | USP | zinc gluconate |
PURAMEX® MG | EP | magnesium lactate |
PURAMEX® ZN | zinc lactate |
Excipients for sustained drug release | ||||||
Products |
Chemical description | Form | HLB | Melting point (°C) (capillary tube) | Drop point (°C) (Mettler) | Techniques |
Compritol® 888 | Glycerol dibehenate EP Glyceryl dibehenate NF Glyceryl behenate Ch.P. |
Powder* Pellets |
2 | 65.0-77.0 | 69.0-74.0 | Direct compression Wet granulation Solid dispersion/ granulation Extrusion (melt/partial melt) Spray cooling/prilling Melt coating |
Gattefossé excipients for lubrication | ||||
Products |
Chemical description | Form | HLB | Drop point (°C) (Mettler) |
Tablet lubricant | ||||
Compritol® 888 ATO | Glycerol dibehenate EP Glyceryl dibehenate NF Glyceryl behenate Ch.P. | Powder* | 2 | 69.0-74.0 |
Compritol® HD5 ATO | Behenoyl polyoxyl-8 glycerides NF | Powder* | 5 | 60.0-67.0 |
Excipients for taste masking and API protection | ||||||
Products |
Chemical description | Form | HLB | Melting point (°C) (capillary tube) | Drop point (°C) (Mettler) | Techniques |
Taste Masking | ||||||
Precirol® ATO 5 | Glycerol distearate (type I) EP Glyceryl distearate NF |
Powder* | 2 | 50.0-60.0 | 53.0-57.0 | Hot melt coating Melt granulation Extrusion (melt/ partial melt) |
Geleol™Mono and diglycerides NF | Glycerol monostearate 40-55 (type I) EP Mono and Diglycerides NF |
Pellets | 3 | 54.0-64.0 | 54.5-64.5 | Melt granulation Extrusion (melt/ partial melt) |
API protection / API compatibility | ||||||
Compritol® 888 ATO | Glycerol dibehenate EP Glyceryl dibehenate NF Glyceryl behenate Ch.P. |
Powder* | 2 | 65.0-77.0 | 69.0-74.0 | Hot melt coating Melt granulation Extrusion (melt/ partial melt) |