Source: Web Search Revision Year: 2017
| Tablets 0.1 mg | OD Tablets 0.1 mg | ||
|---|---|---|---|
| Active ingredient Content per tablet | Imidafenacin 0.1 mg | Imidafenacin 0.1 mg | |
| Inactive ingredients | Microcrystalline cellulose, Partly pregelatinized starch, Povidone, Magnesium stearate, Hypromellose, Titanium oxide, Red ferric oxide, Carnauba wax | Partly pregelatinized starch, Aminoalkyl methacrylate copolymer E, Magnesium stearate, D-Mannitol, Crospovidone, Hydrated silicon dioxide | |
| Type of tablet | Film-coated tablets | Plain tablets (orally disintegrating tablets) | |
| Color | Pale red to reddish brown or pale reddish violet | White | |
| Size | Diameter | 7.1 mm | 7.6 mm |
| Thickness | 3.5 mm | 4.1 mm | |
| Weight | 140 mg | 180 mg | |
| Identification code | URITOS 0.1 (tablet) KP-197 (package) | KP-121 | |
Nonproprietary name: Imidafenacin (JAN)
Chemical name: 4-(2-Methyl-1H-imidazol-1-yl)-2,2-diphenylbutanamide
Molecular formula: C20H21N3O
Molecular weight: 319.40
Melting point: 192 to 196°C
Description: Imidafenacin occurs as a white crystal or crystalline powder. It is freely soluble in acetic acid (100), soluble in N,N-dimethyl formamide (DMF) and methanol, sparingly soluble in ethanol (99.5), slightly soluble in acetonitrile, and practically insoluble in water.
Partition coefficient:
| Organic phase | Aqueous phase | Partition coefficient |
|---|---|---|
| 1-Octanol | pH4.03 (McIlvaine’s buffer) | 0.0664 |
| 1-Octanol | pH6.08 (McIlvaine’s buffer) | 4.47 |
| 1-Octanol | pH8.07 (McIlvaine’s buffer) | 240 |
| How Supplied |
|---|
|
URITOS Tablets 0.1 mg: PTP package: 100 tablets (10 tablets × 10) Non-sealed package: 500 tablets URITOS OD Tablets 0.1 mg: PTP package: 100 tablets (10 tablets × 10) Storage conditions: Protect from moisture after opening aluminum package. Manufactured and marketed by: Kyorin Pharmaceutical Co., Ltd. 6, Kanda surugadai 4-chome, Chiyoda-ku, Tokyo 101-8311, Japan |
| Drug | Countries | |
|---|---|---|
| URITOS | Ecuador, Japan |
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