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PHARMATRANS SANAQ AG is specialized in pharmaceutical excipients in solid dosage forms. Next to standard binders, fillers, lubricants and disintegrants, Pharmatrans offers innovative solutions for DDS based on neutral and functional starter cores as well as for ODT.

From its headquarter in Allschwil-Basel/Switzerland Pharmatrans mainly serves the industry in Europe, India, Asia and South America with local support of its customers.

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Sugar Spheres SANAQ® are neutral pellets made of Sucrose and maize starch according to the monographies for “Sugar Spheres” – NF, Ph. Eur. and JP. The almost spherical cores are used as a neutral basis for the production of Pellets loaded with API.


SUGAR SPHERES SANAQ

Combination of two or more compendial or non-compendial excipients designed to physically modify their properties without chemical change not leading to the formation of covalent bonds. The combination and selction of ingredients is designed to maximize performance their functionality.


DiCOM SANAQ

Pellets made of Microcristalline Cellulose for retard formulations and innovative drug delivery. According to monographs of Microcrystalline Cellulose (Ph. Eur., USP-NF). DMF N° 18519 since July 15, 2005.

A homogeneous distribution of the active agend and the controlled release are two fundamental advantages of this dosage form.

Multiple dosage form mean more reliable formulations thanks to the homogeneous concentration of highly active agents. CELLETS® support this pioneering development. We can supply this innovative pellet in almost any particle size starting from 100 µm micropellets.


CELLETS

LubriSanaq® is a problem solver when other lubricating agents fail to provide tablets of adequate stability, hardness, content uniformity and show difficulties with disintegration and dissolution rates.LubriSanaq® is used as a lubricant in capsules and tablet formulations at 0.25 – 3.0 % w/w concentrations.


LubriSanaq

Sodium Starch Glycolate SSG SANAQ®, the sodium starch glycolate of potato starch, is a chemically modified (sodium hydroxide and chloride acid) derivative of starch.SSG SANAQ® is used as disintegrant for tablets, capsules and granules. The tablets mainly are produced by direct tableting and wet granulation.SSG SANAQ® is recommended in a concentration of 2-8% of the total weight.SSG SANAQ® is a starch derivative, which chemical and physical identities meed the latest standards of (Ph. Eur., USP-NF, BP).


SSG SANAQ

TAP® – Tartaric Acid Pellets

Tartaric Acid is widely used in food products, oral, topical an paranteral pharmaceutical formulations and is generally regarded as a nontoxic and nonirritant material.

In general tartaric acid is also used:


	in beverages, confectionery, food products and pharmaceutical formulations as an acidulant
	as a sequesterring agent
	as an antioxidant synergist
	in pharmaceutical formulations with bicarbonates, as the acid component of effervescent granules, powders and tablets



Ibuprofen are spherically shaped particles consisting of 100 % Ibuprofen drug substance. Ibuprofen DC 100 is the unique directly compressible form of Ibuprofen which consists of 100 % pure drug substance with no additional excipients. Due to its shape and surface structure Ibuprofen DC 100 provides unique product characteristics offering a wide range of applications.


IBUPROFEN DC 100

Microcrystalline Cellulose MCC SANAQ® S is a purified and partially depolymerized α-cellulose. High standards in the selection of the raw material and the ingredients for the production of MCC SANAQ® S and strict observation of the manufacturing guarantee a steady quality.


MCC SANAQ® S

PVP SANAQ® is a hygroscopic, amorphous powder, which is in medicaments (especially tablets) usually used as a binder and can affect the release of the drug into the body. The crosslinked products controll the disintegration of the tablet.

Due to its amorphous structure PVP has no melting point, but a glass transition temperature, depending of the polymerisation between 110 and 180 °C.PVP SANAQ® dissolves in water and in a variety of organic solvents.


PVP SANAQ

SSG SANAQ® Type A is Blue color with iodine reagent

SSG SANAQ® Type A

CELLETS® 500 has shorter and more stable layering process with high yields due to low friability and non-solubility in comparison to standard starter cores.

CELLETS® 500

Microcrystalline Cellulose is purified, partially depolymerized cellulose prepared by treating alpha cellulose, obtained as a pulp from fibrous plant material, with mineral acids

MCC SANAQ® 102

TAP® 425 - 500 is tartaric acid pellet, white or beige in color. These pellets are optimized for coating and layering processes to achieve reproducible product characteristics.

TAP® 425 - 500

CELLETS® 263 is highly spherical and narrow particle size for reproducible production process and content uniformity.

CELLETS® 263

CELLETS® 780 is smallest size starter core(<200 μm) for the production of micropellets and MUPS tablet formulation incl.ODT.

CELLETS® 780

CELLETS® 200 is highly spherical and narrow particle size for reproducible production process and content uniformity.

CELLETS® 200

TAP® 300 - 425 is tartaric acid pellet, white or beige in color. These pellets are optimized for coating and layering processes to achieve reproducible product characteristics.

TAP® 300 - 425

CELLETS® 350 has shorter and more stable layering process with high yields due to low friability and non-solubility in comparison to standard starter cores.

CELLETS® 350

PHARMATRANS SANAQ AG

PHARMATRANS SANAQ AG is specialized in pharmaceutical excipients in solid dosage forms. Next to standard binders, fillers, lubricants and disintegrants, Pharmatrans offers innovative solutions for DDS

PHARMATRANS SANAQ AG - Knowde

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SSG SANAQ® Technical Data Sheet

SSG SANAQ® Technical Data Sheet - PHARMATRANS SANAQ AG

SSG SANAQ® Type A Safety Data Sheet

SSG SANAQ® Type A Safety Data Sheet - PHARMATRANS SANAQ AG

SSG SANAQ Type A - PHARMATRANS SANAQ AG - 9063-38-1 - EP - Knowde

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	Value	Units	Test Method / Conditions
Sodium Chloride	max. 7	%	USP/NF / Ph. EUR / JPE
Sodium Glycolate	max. 2	%	USP/NF / Ph. EUR / JPE
Iron	max. 20	ppm	USP/NF / Ph. EUR / JPE
Loss on Drying	max. 10	%	USP/NF / Ph. EUR / JPE
Microbial Contamination	2.8 - 4.2	%	USP/NF / Ph. EUR / JPE
Assay	400	—	USP/NF / Ph. EUR / JPE
Residual Solvent (methanol)	max. 3000	ppm	USP/NF / Ph. EUR / JPE

SSG SANAQ® Type A

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