1642857
USP
Tacrolimus System Suitability Mixture
United States Pharmacopeia (USP) Reference Standard
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About This Item
Recommended Products
grade
pharmaceutical primary standard
API family
tacrolimus
manufacturer/tradename
USP
application(s)
pharmaceutical (small molecule)
format
mixture
storage temp.
−20°C
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.
For further information and support please go to the website of the issuing Pharmacopoeia.
Application
Tacrolimus System Suitability Mixture USP reference standard for use in specified quality tests and assays.
Also used to prepare system suitability solution for assay and impurities analysis using liquid chromatography method and UV detector according to the given below monographs of United States Pharmacopeia (USP):
Also used to prepare system suitability solution for assay and impurities analysis using liquid chromatography method and UV detector according to the given below monographs of United States Pharmacopeia (USP):
- Tacrolimus Capsules
- Tacrolimus
Analysis Note
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
Other Notes
Sales restrictions may apply.
related product
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Repr. 2 - STOT RE 2
Storage Class Code
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Certificates of Analysis (COA)
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Tacrolimus
United States Pharmacopeia, 41(2), 4193-4193 (2021)
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