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Inactive Ingredient Search for Approved Drug Products

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

Quarter Inactive Ingredient Route of Administration Dosage Form Maximum Potency per unit dose Maximum Daily Exposure Status
182960 Q4 2022 LACTOSE MONOHYDRATE VAGINAL TABLET, FILM COATED 17.90 mg Deletion
183077 Q3 2022 LACTOSE MONOHYDRATE VAGINAL INSERT 210.00 mg MDE Replacement
183078 Q4 2022 LACTOSE MONOHYDRATE VAGINAL INSERT 630mg MDE Replacement
183079 Q3 2022 LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE ORAL TABLET, FILM COATED 40.00 mg MDE Replacement
183080 Q4 2022 LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE ORAL TABLET, FILM COATED 40mg 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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