USFDA APPLICATION NUMBER - 21306 / DOSAGE - FILM, EXTENDED RELEASE;TRANSDERMAL - 10MCG/HR
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
buprenorphine(UNII: 40D3SCR4GZ) (buprenorphine - UNII:40D3SCR4GZ) | buprenorphine | 20ug in 1 | 10ug in 1 | 5ug in 1 |
Inactive Ingredients
Ingredient Name | A-S Medication Solutions LLC | Lake Erie Medical DBA Quality Care Products LLC | Purdue Pharma LP | Rhodes Pharmaceuticals L.P. | Teva Pharmaceuticals USA, Inc. | Apotex Corp. | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
---|---|---|---|---|---|---|---|
ethyl levulinate(7BU24CSS2G) | |||||||
levulinic acid(RYX5QG61EI) | |||||||
oleyl oleate(3X3L452Y85) | |||||||
POVIDONE(FZ989GH94E) | |||||||
POVIDONE, UNSPECIFIED(FZ989GH94E) |
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