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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
312734 Q1 2024 LECITHIN, SOYBEAN ORAL CAPSULE 20.00 mg Correction
312736 Q1 2024 LECITHIN, SOYBEAN ORAL POWDER, FOR SUSPENSION 39mg Correction
312738 Q1 2024 LECITHIN, SOYBEAN ORAL TABLET 8mg Correction
312740 Q1 2024 LECITHIN, SOYBEAN ORAL TABLET, EXTENDED RELEASE 20mg Correction
312742 Q1 2024 LECITHIN, SOYBEAN ORAL TABLET, FILM COATED 0.33 mg Correction
312744 Q1 2024 LECITHIN, SOYBEAN RESPIRATORY (INHALATION) AEROSOL, METERED 0.10 %w/w Correction
312746 Q1 2024 LECITHIN, SOYBEAN VAGINAL CREAM 1.00 %w/w Correction
312811 Q1 2024 LACTOSE MONOHYDRATE ORAL CAPSULE, EXTENDED RELEASE 536.40 mg MDE Replacement
312812 Q2 2024 LACTOSE MONOHYDRATE ORAL CAPSULE, EXTENDED RELEASE 5364mg MDE Replacement
312813 Q1 2024 LANOLIN RECTAL OINTMENT 14.00 %w/w MDE Replacement
312814 Q2 2024 LANOLIN RECTAL OINTMENT 105mg MDE Replacement
312815 Q1 2024 LAURYL LACTATE TRANSDERMAL FILM, EXTENDED RELEASE 12.00 mg MDE Replacement
312816 Q2 2024 LAURYL LACTATE TRANSDERMAL FILM, EXTENDED RELEASE 12mg 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: March 15, 2024
Database Last Updated: April 29, 2024

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