Product NDC: | 67919-020 |
Proprietary Name: | Entereg |
Non Proprietary Name: | alvimopan |
Active Ingredient(s): | 12 mg/1 & nbsp; alvimopan |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67919-020 |
Labeler Name: | Cubist Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021775 |
Marketing Category: | NDA |
Start Marketing Date: | 20120416 |
Package NDC: | 67919-020-10 |
Package Description: | 6 BLISTER PACK in 1 CARTON (67919-020-10) > 5 CAPSULE in 1 BLISTER PACK |
NDC Code | 67919-020-10 |
Proprietary Name | Entereg |
Package Description | 6 BLISTER PACK in 1 CARTON (67919-020-10) > 5 CAPSULE in 1 BLISTER PACK |
Product NDC | 67919-020 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | alvimopan |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20120416 |
Marketing Category Name | NDA |
Labeler Name | Cubist Pharmaceuticals, Inc. |
Substance Name | ALVIMOPAN |
Strength Number | 12 |
Strength Unit | mg/1 |
Pharmaceutical Classes |