MEDIOCON INC supplies DigeLact AB Drops as a specialized digestive-enzyme raw material/formulation intended for nutritional and digestive-support applications.
DigeLact AB is associated with alpha-galactosidase (α-galactosidase), an enzyme that hydrolyzes certain α-galactosidic carbohydrates. Alpha-galactosidase is commonly used in digestive-enzyme formulations and food-processing applications.
The exact enzyme source, activity, concentration, carrier system, microbial origin and storage conditions for DigeLact AB Drops should be confirmed from the current product specification and batch COA.
MEDIOCON INC supplies DigeLact AB Drops according to the applicable technical specification, packaging requirements and quality documentation.
Alpha-galactosidase is an enzyme that acts on α-galactosidic bonds in certain carbohydrates.
DigeLact AB Drops are presented as a liquid/drop preparation, making the format suitable for controlled incorporation into appropriate nutritional formulations.
For enzyme products, activity units are more meaningful than simply reporting percentage purity. The exact activity should therefore be taken from the current product specification and COA.
DigeLact AB Drops may be used in:
Specific digestive or health claims should only be used when supported by appropriate evidence, product documentation and applicable regulations.
| Parameter | Specification |
|---|---|
| Appearance | Clear to slightly colored liquid, depending on formulation |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying DigeLact AB Drops Manufacturer & Supplier in India | MEDIOCON INC (CAS 9025-35-8*) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our DigeLact AB Drops Manufacturer & Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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