Saxagliptin impurity mixture

Description

• General description: This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.
• Application: Saxagliptin impurity mixture EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.
• Packaging: Unit quantity: 0.004mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
• Other Notes: Sales restrictions may apply.