USFDA APPLICATION NUMBER - 22204 / DOSAGE - GEL;TRANSDERMAL - 10% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
OXYBUTYNIN CHLORIDE(UNII: L9F3D9RENQ) (OXYBUTYNIN - UNII:K9P6MC7092) | OXYBUTYNIN CHLORIDE | 100mg in 1 |
Inactive Ingredients
Ingredient Name | Actavis Pharma, Inc. |
---|---|
ALCOHOL(3K9958V90M) | |
GLYCERIN(PDC6A3C0OX) | |
HYDROXYPROPYL CELLULOSE (TYPE H)(RFW2ET671P) | |
SODIUM HYDROXIDE(55X04QC32I) | |
WATER(059QF0KO0R) |
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