Development and validation of a dissolution test for empagliflozin in film-coated tablets
The present study proposes a validated dissolution method for empagliflozin (EMPA) in film coated tablets. A gradual in vitro dissolution profile for this formulation was obtained using 900 mL of hydrochloric acid 0.01 M at 37 °C ± 0.5 °C as dissolution medium and USP apparatus 2 (paddle) at 50 rpm...
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Universidade Federal do Rio Grande do Sul
2021-12-01
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| Series: | Drug Analytical Research |
| Online Access: | https://seer.ufrgs.br/index.php/dar/article/view/112077 |
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Development and validation of a dissolution test for empagliflozin in film-coated tablets
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Development and validation of a dissolution test for empagliflozin in film-coated tablets
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Development and validation of a dissolution test for empagliflozin in film-coated tablets
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Development and validation of a dissolution test for empagliflozin in film-coated tablets
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