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List of Inactive Ingredients used to produce Sucralose API listed on PharmaCompass with Finished Dosage Forms (Formulations)

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01 FILM, SOLUBLE (1)

02 GRANULE (1)

03 GRANULE, FOR ORAL SUSPENSION (1)

04 GUM, CHEWING (1)

05 LIQUID (1)

06 POWDER, FOR ORAL SOLUTION (1)

07 POWDER, FOR ORAL SUSPENSION (1)

08 POWDER, FOR SOLUTION (1)

09 SOLUTION (1)

10 SPRAY (1)

11 SPRAY, METERED (1)

12 SUSPENSION (1)

13 SUSPENSION, EXTENDED RELEASE (1)

14 SYRUP (1)

15 TABLET (3)

16 TABLET (IMMED./COMP. RELEASE), UNCOATED, BUCCAL (1)

17 TABLET (IMMED./COMP. RELEASE), UNCOATED, CHEWABLE (2)

18 TABLET, CHEWABLE (1)

19 TABLET, EFFERVESCENT, FOR SOLUTION (1)

20 TABLET, ORALLY DISINTEGRATING (1)

21 TABLET, UNCOATED, LOZENGE (2)

22 TROCHE (1)

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01 0.018 (1)

02 0.15 (2)

03 0.2 (1)

04 0.52 (1)

05 0.65 (1)

06 0.76 (1)

07 1 (1)

08 1.3 (1)

09 1.5 (1)

10 1.88 (1)

11 2 (1)

12 2.33 (1)

13 3.5 (2)

14 4 (1)

15 5.4 (1)

16 5.5 (1)

17 5.75 (1)

18 15 (1)

19 30 (1)

20 34.25 (1)

21 40 (2)

22 90 (1)

23 1210 (1)

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GUM, CHEWING
BUCCAL
56038132
96K6UQ3ZD4
3.5
MG
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FDA INACTIVE INGREDIENT DATABASE

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SPRAY
NASAL
56038132
96K6UQ3ZD4
0.15
%
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FDA INACTIVE INGREDIENT DATABASE

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SPRAY, METERED
NASAL
56038132
96K6UQ3ZD4
0.15
%
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FDA INACTIVE INGREDIENT DATABASE

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FILM, SOLUBLE
ORAL
56038132
96K6UQ3ZD4
5.5
MG
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GRANULE
ORAL
56038132
96K6UQ3ZD4
5.4
MG
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GRANULE, FOR ORAL SUSP...
ORAL
56038132
96K6UQ3ZD4
2.33
MG
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LIQUID
ORAL
56038132
96K6UQ3ZD4
1
MG/1ML
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POWDER, FOR ORAL SOLUT...
ORAL
56038132
96K6UQ3ZD4
1210
MG
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POWDER, FOR ORAL SUSPE...
ORAL
56038132
96K6UQ3ZD4
90
MG/1PKT
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POWDER, FOR SOLUTION
ORAL
56038132
96K6UQ3ZD4
34.25
MG
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