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Inactive Ingredient Search for Approved Drug Products

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

Quarter Inactive Ingredient Route of Administration Dosage Form Maximum Potency per unit dose Maximum Daily Exposure Status
182823 Q4 2022 FLAVOR CHERRY FT-9496 ORAL SOLUTION 200mg Correction
182953 Q3 2022 FLAVOR GRAPE 61.13252 ORAL SYRUP 2.00 mg/ 1.00 ml 20mg Deletion
183047 Q3 2022 FD&C BLUE NO. 1 ORAL CAPSULE, EXTENDED RELEASE 1.32 mg MDE Replacement
183048 Q4 2022 FD&C BLUE NO. 1 ORAL CAPSULE, EXTENDED RELEASE 1mg MDE Replacement
183049 Q3 2022 FD&C BLUE NO. 2--ALUMINUM LAKE ORAL TABLET, ORALLY DISINTEGRATING 4.70 mg MDE Replacement
183050 Q4 2022 FD&C BLUE NO. 2--ALUMINUM LAKE ORAL TABLET, ORALLY DISINTEGRATING 38mg MDE Replacement
183051 Q3 2022 FD&C GREEN NO. 3 ORAL TABLET 10.00 mg MDE Replacement
183052 Q4 2022 FD&C GREEN NO. 3 ORAL TABLET 240mg MDE Replacement
183053 Q3 2022 FLAVOR RASPBERRY 28106 ORAL SUSPENSION/ DROPS 5.00 mg/ 1.00 ml MDE Replacement
183054 Q4 2022 FLAVOR RASPBERRY 28106 ORAL SUSPENSION/ DROPS 38mg 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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