Unique Ingredient Identifier 5856J3G2A2 is listed as a ingredient substance
| RN | 9063-38-1 |
| RXCUI | 1366849 |
UNII 5856J3G2A2 SODIUM STARCH GLYCOLATE TYPE A POTATO is commonly included in medications in the following forms.
| Route | Dosage Form | Potency |
|---|---|---|
| ORAL | TABLET | 70 mg |
| ORAL | TABLET, DELAYED RELEASE | 36 mg |
| ORAL | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE | 19.88 mg |
| BUCCAL | TABLET | 8.3 MG |
| ORAL | CAPSULE | 180 MG |
| ORAL | CAPSULE, COATED PELLETS | 16.71 MG |
| ORAL | CAPSULE, DELAYED ACTION | 15 MG |
| ORAL | CAPSULE, DELAYED ACTION, COATED, HARD GELATIN | 16 MG |
| ORAL | CAPSULE, DELAYED RELEASE | 18.3 MG |
| ORAL | CAPSULE, ENTERIC COATED PELLETS | 16.8 MG |
| ORAL | CAPSULE, EXTENDED RELEASE | 30 MG |
| ORAL | CAPSULE, HARD GELATIN | 20 MG |
| ORAL | CAPSULE, SOFT GELATIN | 7.75 MG |
| ORAL | CAPSULE, SUSTAINED ACTION | 18.6 MG |
| ORAL | DISPERSIBLE TABLET | 2.4 MG |
| ORAL | TABLET | 876 MG |
| ORAL | TABLET (IMMED./COMP. RELEASE), COATED | 17 MG |
| ORAL | TABLET (IMMED./COMP. RELEASE), FILM COATED | 20 MG |
| ORAL | TABLET (IMMED./COMP. RELEASE), UNCOATED, CHEWABLE | 50 MG |
| ORAL | TABLET, CHEWABLE | 75 MG |
| ORAL | TABLET, COATED | 73 MG |
| ORAL | TABLET, CONTROLLED RELEASE | 25.86 MG |
| ORAL | TABLET, DELAYED ACTION | 34 MG |
| ORAL | TABLET, DELAYED ACTION, ENTERIC COATED | 21 MG |
| ORAL | TABLET, DELAYED RELEASE | 60.5 MG |
| ORAL | TABLET, ENTERIC COATED PARTICLES | 12 MG |
| ORAL | TABLET, EXTENDED RELEASE | 48 MG |
| ORAL | TABLET, FILM COATED | 90 MG |
| ORAL | TABLET, MULTILAYER, COATED | 2 MG |
| ORAL | TABLET, ORALLY DISINTEGRATING | 71.43 MG |
| ORAL | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE | 3 mg |
| ORAL | TABLET, SUSTAINED ACTION | 15 MG |
| ORAL | TABLET, SUSTAINED ACTION, COATED | NA |
| ORAL | TABLET, SUSTAINED ACTION, FILM COATED | 10 MG |
| SUBLINGUAL | TABLET | 5.5 MG |
| TRANSMUCOSAL | TABLET | 10 MG |