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Inactive Ingredient Search for Approved Drug Products

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

Quarter Inactive Ingredient Route of Administration Dosage Form Maximum Potency per unit dose Maximum Daily Exposure Status
312730 Q1 2024 HYDROXYPROPYL CELLULOSE (1600000 WAMW) ORAL CAPSULE, EXTENDED RELEASE 214mg Correction
312731 Q2 2024 HYDROXYPROPYL CELLULOSE (1600000 WAMW) ORAL CAPSULE, EXTENDED RELEASE 204mg Correction
312732 Q1 2024 HYPROMELLOSE 2910 (4000 MPA.S) OPHTHALMIC GEL 197mg Correction
312733 Q2 2024 HYPROMELLOSE 2910 (4000 MPA.S) OPHTHALMIC GEL 1mg Correction
312769 Q2 2024 HYDROCHLORIC ACID INTRAVENOUS POWDER, FOR SOLUTION ADJ PH Deletion
312770 Q2 2024 HYPROMELLOSE NASAL SPRAY 1.00 mg/ 1.00 ml 1mg Deletion
312771 Q2 2024 HYPROMELLOSE ORAL SOLUTION 3.70 mg/ 1.00 ml Deletion
312807 Q1 2024 HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) OPHTHALMIC SOLUTION/ DROPS 0.48 %w/v MDE Replacement
312808 Q2 2024 HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) OPHTHALMIC SOLUTION/ DROPS 1mg MDE Replacement
312809 Q1 2024 HYPROMELLOSE 2208 (15000 MPA.S) ORAL TABLET 323.28 mg MDE Replacement
312810 Q2 2024 HYPROMELLOSE 2208 (15000 MPA.S) ORAL TABLET 375mg 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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