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Inactive Ingredient Search for Approved Drug Products

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

Quarter Inactive Ingredient Route of Administration Dosage Form Maximum Potency per unit dose Maximum Daily Exposure Status
264927 Q3 2023 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS TOPICAL SOLUTION 0.47 %w/v Deletion
264928 Q3 2023 SORBITOL ORAL SUSPENSION/ DROPS 30.00 mg/ 1.00 ml Deletion
264929 Q3 2023 SORBITOL TOPICAL SOLUTION/ DROPS 6.90 %w/v Deletion
265062 Q2 2023 SODIUM BENZOATE TOPICAL GEL 0.24 %w/w MDE Replacement
265063 Q3 2023 SODIUM BENZOATE TOPICAL GEL 5mg MDE Replacement
265064 Q2 2023 SODIUM BICARBONATE ORAL GUM, CHEWING 15.00 mg MDE Replacement
265065 Q3 2023 SODIUM BICARBONATE ORAL GUM, CHEWING 360mg MDE Replacement
265066 Q2 2023 SODIUM CARBONATE ORAL GUM, CHEWING 10.00 mg MDE Replacement
265067 Q3 2023 SODIUM CARBONATE ORAL GUM, CHEWING 240mg MDE Replacement
265068 Q2 2023 SODIUM CHLORIDE INTRA-ARTERIAL INJECTION, SOLUTION 0.01 %w/v MDE Replacement
265069 Q3 2023 SODIUM CHLORIDE INTRA-ARTERIAL INJECTION, SOLUTION 278mg MDE Replacement
265070 Q2 2023 SODIUM HYDROXIDE VAGINAL GEL 0.25 %w/w MDE Replacement
265071 Q3 2023 SODIUM HYDROXIDE VAGINAL GEL 20mg MDE Replacement
265072 Q2 2023 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS INTRALESIONAL INJECTION, SUSPENSION 0.14 %w/v MDE Replacement
265073 Q3 2023 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS INTRALESIONAL INJECTION, SUSPENSION 3mg MDE Replacement
265074 Q2 2023 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS SOFT TISSUE INJECTION, SUSPENSION 0.14 %w/v MDE Replacement
265075 Q3 2023 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS SOFT TISSUE INJECTION, SUSPENSION 3mg MDE Replacement
265076 Q2 2023 SODIUM PHOSPHATE, DIBASIC, DODECAHYDRATE OPHTHALMIC SOLUTION 1.26 %w/v MDE Replacement
265077 Q3 2023 SODIUM PHOSPHATE, DIBASIC, DODECAHYDRATE OPHTHALMIC SOLUTION 5mg MDE Replacement
265078 Q2 2023 SODIUM PROPIONATE ORAL SYRUP 10.00 mg/ 5.00 ml MDE Replacement
265079 Q3 2023 SODIUM PROPIONATE ORAL SYRUP 40mg MDE Replacement
265080 Q2 2023 SORBIC ACID ORAL SOLUTION 5.00 mg/ 5.00 ml MDE Replacement
265081 Q3 2023 SORBIC ACID ORAL SOLUTION 80mg MDE Replacement
265082 Q2 2023 SORBITAN MONOOLEATE ORAL TABLET, DELAYED RELEASE 1.89 mg MDE Replacement
265083 Q3 2023 SORBITAN MONOOLEATE ORAL TABLET, DELAYED RELEASE 4mg MDE Replacement
265084 Q2 2023 SORBITOL ORAL GUM, CHEWING 257.00 mg MDE Replacement
265085 Q3 2023 SORBITOL ORAL GUM, CHEWING 6168mg MDE Replacement
265086 Q2 2023 STARCH 826 ORAL TABLET 138.00 mg MDE Replacement
265087 Q3 2023 STARCH 826 ORAL TABLET 320mg MDE Replacement
265088 Q2 2023 STARCH, PREGELATINIZED ORAL TABLET, COATED 125.00 mg MDE Replacement
265089 Q3 2023 STARCH, PREGELATINIZED ORAL TABLET, COATED 460mg 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: July 6, 2023
Database Last Updated: July 21, 2023

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