1559505
USP
Prednisone tablets
United States Pharmacopeia (USP) Reference Standard
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About This Item
Recommended Products
grade
pharmaceutical primary standard
API family
prednisone
manufacturer/tradename
USP
application(s)
pharmaceutical (small molecule)
format
neat
General description
Prednisone Tablets is replaced with Dissolution Performance Verification Standard - Prednisone (30 tablets).
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, has 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.
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, has 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
This USP reference standard is intended for use in specified quality tests and assays. It is also used to prepare standard solutions as per USP monograph Prednisone tablets for:
- Confirming the chemical identity in samples by infrared spectroscopy
- System suitability testing of liquid chromatographic and gas chromatographic systems
- Performance verification testing for USP Apparatus 1 and 2 with 1-Liter vessels as per the USP general test chapter on dissolution <711> and drug release <724>, apparatus suitability
- Testing content uniformity of preparations in dosage units
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.
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Certificates of Analysis (COA)
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