Product NDC: | 60760-911 |
Proprietary Name: | Fentanyl |
Non Proprietary Name: | FENTANYL |
Active Ingredient(s): | 25 ug/h & nbsp; FENTANYL |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | PATCH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60760-911 |
Labeler Name: | St. Marys Medical Park Pharmacy |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077062 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110126 |
Package NDC: | 60760-911-05 |
Package Description: | 5 POUCH in 1 CARTON (60760-911-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
NDC Code | 60760-911-05 |
Proprietary Name | Fentanyl |
Package Description | 5 POUCH in 1 CARTON (60760-911-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
Product NDC | 60760-911 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FENTANYL |
Dosage Form Name | PATCH |
Route Name | TRANSDERMAL |
Start Marketing Date | 20110126 |
Marketing Category Name | ANDA |
Labeler Name | St. Marys Medical Park Pharmacy |
Substance Name | FENTANYL |
Strength Number | 25 |
Strength Unit | ug/h |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |