Unique Ingredient Identifier O8232NY3SJ is listed as a ingredient substance
RN | 9005-25-8 |
NCIT | C80778 |
RXCUI | 1039062 |
UNII O8232NY3SJ STARCH, CORN is commonly included in medications in the following forms.
Route | Dosage Form | Potency |
---|---|---|
ORAL | CAPSULE | 70 mg |
ORAL | TABLET | 128.06 mg |
ORAL | TABLET, FILM COATED | 68.4 mg |
BUCCAL | TABLET | 16.6 MG |
ORAL | CAPSULE | 600 MG |
ORAL | CAPSULE (IMMED./COMP. RELEASE) | 110 MG |
ORAL | CAPSULE, COATED, SOFT GELATIN | 27.75 MG |
ORAL | CAPSULE, DELAYED ACTION | 36.4 MG |
ORAL | CAPSULE, DELAYED RELEASE | 36 MG |
ORAL | CAPSULE, EXTENDED RELEASE | 95.85 MG |
ORAL | CAPSULE, HARD GELATIN | 289.2 MG |
ORAL | CAPSULE, SUSTAINED ACTION | 27 MG |
ORAL | CONCENTRATE | NA |
ORAL | DROPS | NA |
ORAL | LIQUID,EXTENDED RELEASE | 9.38 MG/ML |
ORAL | PASTILLE | NA |
ORAL | POWDER, FOR ORAL SUSPENSION | 16.85 MG/5ML |
ORAL | POWDER, FOR SUSPENSION | NA |
ORAL | SUSPENSION | 72.5 MG/5ML |
ORAL | SUSPENSION, DROPS | NA |
ORAL | TABLET | 482 MG |
ORAL | TABLET (IMMED./COMP. RELEASE), COATED | 28 MG |
ORAL | TABLET (IMMED./COMP. RELEASE), FILM COATED | 24 MG |
ORAL | TABLET (IMMED./COMP. RELEASE), UNCOATED, CHEWABLE | 170 MG |
ORAL | TABLET, CHEWABLE | 30 MG |
ORAL | TABLET, COATED | 285 MG |
ORAL | TABLET, DELAYED ACTION | 101.8 MG |
ORAL | TABLET, DELAYED ACTION, ENTERIC COATED | 54 MG |
ORAL | TABLET, DELAYED RELEASE | 15 MG |
ORAL | TABLET, EXTENDED RELEASE | 250 MG |
ORAL | TABLET, FILM COATED | 232 MG |
ORAL | TABLET, MULTILAYER, EXTENDED RELEASE | 10 MG |
ORAL | TABLET, ORALLY DISINTEGRATING | 45 MG |
ORAL | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE | 3.48 mg |
ORAL | TABLET, REPEAT ACTION | 32 MG |
ORAL | TABLET, SUSTAINED ACTION | 92 MG |
ORAL | TABLET, SUSTAINED ACTION, COATED | NA |
ORAL | TABLET, SUSTAINED ACTION, FILM COATED | 74.3 MG |
SUBLINGUAL | TABLET | 136.44 MG |
SUBLINGUAL | TABLET (IMMED./COMP. RELEASE), UNCOATED, BUCCAL | 32 MG |
VAGINAL | TABLET | 210 MG |
VAGINAL | TABLET, FILM COATED | 8 MG |
ORAL | TABLET | 106.72 mg |