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Inactive Ingredient Search for Approved Drug Products

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

Quarter Inactive Ingredient Route of Administration Dosage Form Maximum Potency per unit dose Maximum Daily Exposure Status
138109 Q3 2022 ICODEXTRIN ORAL POWDER, FOR SOLUTION 12.50 mg/ 5.00 ml Deletion
138111 Q3 2022 INK BLACK SW-9009 ORAL CAPSULE, EXTENDED RELEASE NA Deletion

 

 

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: July 1, 2022
Database Last Updated: July 18, 2022

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