		Zielsetzung	Verfallsdatum
.AspNetCore.Mvc.CookieTempDataProvider	dfepharma.com	Bewahrt den Sitzungsstatus des Besuchers über Seitenanfragen hinweg.	Sitzung	HTTP
.AspNetCore.Antiforgery	dfepharma.com	Hilft bei der Verhinderung von CSRF-Angriffen (Cross-Site Request Forgery).	Sitzung	HTTP
formulierung-werkzeug-senden-ratschlag-zu-selbst	dfepharma.com	So bearbeiten Sie eine Anfrage zum Senden von Ratschlägen an Sie selbst.	Sitzung	HTTP
formulierungs-werkzeug-anforderung-muster	dfepharma.com	Zur Bearbeitung einer Musteranforderung.	Sitzung	HTTP
UMB_SESSION	dfepharma.com	Bewahrt den Sitzungsstatus des Besuchers über Seitenanfragen hinweg.	Sitzung	HTTP
ARRAffinitySameSite	dfepharma.com	Wird verwendet, um den Datenverkehr auf der Website auf mehrere Server zu verteilen, um die Antwortzeiten zu optimieren.	Sitzung	HTTP
AWSALBCORS	rocketfuel.humanfirstdigital.agency	Registriert eine eindeutige ID, die verwendet wird, um statistische Daten darüber zu erstellen, wie der Besucher die Website nutzt.	Eine Woche	HTTP
Angebotsformular	dfepharma.com	Um eine Angebotsanfrage zu bearbeiten.	Eine Woche	HTTP
Muster anfordern	dfepharma.com	Zur Bearbeitung einer Musteranforderung.	Eine Woche	HTTP

Pharmatose® 200M NZ

Hochgradig konsistente Monohydrat-Laktose

Gute Verdichtungseigenschaften,

Angebote von mehreren Produktionsstandorten

Orale feste Darreichungsformen

Produktinformation

Pharmatose® und Lactochem® sind die Markennamen von DFE Pharma für reine, weiße und hochkristalline, gemahlene Monohydratqualitäten.

Laktose wird mechanisch zu unterschiedlichen Partikelgrößen gemahlen, so dass Pharmaunternehmen die Qualität wählen können, die am besten zu ihren Formulierungsanforderungen passt. Aufgrund ihrer feinen Beschaffenheit und relativ großen Oberfläche lässt sich gemahlene Laktose gut verdichten. Dieser Laktosetyp wird typischerweise in Tabletten, Kapseln und bei der Extrusionsspheronisierung verwendet.

: Gemahlene Laktose
Funktionalität des Hilfsstoffs: Füllstoff-Bindemittel, Verdünnungsmittel, Bindemittel
Empfohlenes Verfahren: Nassgranulation, Trockenes Mischen, Extrusionsspheronisation, Kontinuierliche Verarbeitung
Darreichungsformen: Tablette, Kapsel (orale Feststoffdosis)

Typische Produktdaten

Partikelgrößenverteilung (μm)

X10: 4
X50: 30
X90: 110

Rohdichte (g/L)

Rohdichte (g/L): 564

Hausner-Verhältnis (-)

Hausner-Verhältnis (-): 1.28

Dokumentation

ALBA Pharmazeutische Laktose
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Oral Solid Dose Brochure Ansehen
Kontaminantenangabe Pharmatose, Respitose und SuperTab (EU)
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FSSC 22000 Fonterra Kapuni
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GVO-Erklärung Laktose
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Halal NZIDT Fonterra Kapuni NZ
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Halal NZIDT DMV-Fonterra Excipients Kaponga NZ
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Halal (MUI) DMV Fonterra Excipients Kapuni NZ
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Halal (MUI) Fonterra Kapuni NZ
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ISO 14001 Fonterra Limited Kapuni NZ
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ISO 9001 DMV Fonterra-Hilfsstoffe Kaponga
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ISO 9001 Fonterra Kapuni
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ISO 9001 DFE Kaponga
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ICHQ3D Elementare Verunreinigungen Laktose EU und NZ
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Inhaltsstoffdeklaration Laktose
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Nährwertangaben Laktose
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Produktspezifikation Pharmatose 200 NZ
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Process Flow Sheet (PFS) Milled lactose Ansehen
Prozessablaufplan Pharmatose 200M NZ
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Welt-Anti-Doping-Code
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Ungefährlicher Stoff
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cGMP-Erklärung
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BSE-Erklärung Laktose & Inhalation
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Bestrahlungsfrei
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Änderungsmanagement
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Dioxin-Erklärung Laktose
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Erklärung zum Produktionsstandort
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Frei von Maul- und Klauenseuche Laktose (NZ)
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Datenintegrität
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Eignungszertifikat
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Inhaltsstoffdeklaration Pharmacel sMCC
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Konformitätserklärung Verpackung
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REACH-Erklärung
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Erklärung zur Betriebskontinuitätsplanung
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Herkunft der Milch
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Abwesenheit von Melamin Laktose
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Restlösungsmittel Laktose
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Haltbarkeitsangabe Lactose
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3. This will open a new browser window with an empty document. Click on "Save". The document will be saved to your computer.
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Wet granulation of milled lactose Ansehen
Re-compaction properties of lactose and mcc Ansehen
Impact of excipient and blend properties on feeding consistency for continuous manufacturing Ansehen

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