Product NDC: | 35356-638 |
Proprietary Name: | FENTANYL TRANSDERMAL SYSTEM |
Non Proprietary Name: | fentanyl transdermal system |
Active Ingredient(s): | 75 ug/h & nbsp; fentanyl transdermal system |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | PATCH, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-638 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077154 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110606 |
Package NDC: | 35356-638-05 |
Package Description: | 5 POUCH in 1 CARTON (35356-638-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
NDC Code | 35356-638-05 |
Proprietary Name | FENTANYL TRANSDERMAL SYSTEM |
Package Description | 5 POUCH in 1 CARTON (35356-638-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
Product NDC | 35356-638 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fentanyl transdermal system |
Dosage Form Name | PATCH, EXTENDED RELEASE |
Route Name | TRANSDERMAL |
Start Marketing Date | 20110606 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | FENTANYL |
Strength Number | 75 |
Strength Unit | ug/h |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |