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DiCom SANAQ® ML 011

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Description

Indicated to aid processing during manufacture, enhance the stability and effectiveness during manufacturing product process. Mixtures with high compressibility,superior diluition properties and fast disintegrating time. The purpose of the excipient is to aid processing during manufacture, enhance stability or bioavailability.

Main Application

Co-processed excipient based on lactose monohydrate and cellulose micro crystalline.

  • Smooth surface of the resulting tablets
  • It provides superior tablet hardness and powder flowability
  • Excellent compaction excipient for sensitive APIs
  • Useful excipient for low dosage formulations
  • Consistent tablet hardness
  • High weight consistency at all compaction speeds

Flow properties

DiCom SANAQ ML 011® shows excellent and superior free powder flow compared with physical mixture in same ratio of components showing very poor flow properties.

PSD

DiCom SANAQ® ML 011 has an average PSD of 300 – 550 microns.

Additional information

Manufacturer

Pharmatrans SANAQ

Quality

EP, JP, USP

Cas-No

64044-51-5, 9004-34-6

Composition

Microcrystalline Cellulose, Starch

Function

Co-Processed

Compendial Name

Microcrstalline Cellulose (USP) / Lactose Monohydrate (USP)

Documents and Links

Sanaq ML 011_Specification

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