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Inactive Ingredient Search for Approved Drug Products

You are Searching: Change and Deletion by Inactive Ingredient Name Beginning with E

Quarter Inactive Ingredient Route of Administration Dosage Form Maximum Potency per unit dose Maximum Daily Exposure Status
182951 Q4 2022 ETHYLCELLULOSE (10 MPA.S) ORAL LIQUID, EXTENDED RELEASE 4.17 mg/ 1.00 ml 50mg Deletion
182952 Q4 2022 ETHYLCELLULOSE (20 MPA.S) ORAL POWDER 298.50 mg Deletion
183045 Q3 2022 EDETATE CALCIUM DISODIUM INTRAVENOUS INJECTION 2.16 mg MDE Replacement
183046 Q4 2022 EDETATE CALCIUM DISODIUM INTRAVENOUS INJECTION 23mg MDE Replacement

 

 

FDA/Center for Drug Evaluation and Research
Office of Pharmaceutical Quality
Office of Policy for Pharmaceutical Quality
Mailbox for IID corrections: IIDUpdate@fda.hhs.gov
Update Frequency: Quarterly

Data Through: October 1, 2022
Database Last Updated: October 19, 2022

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