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FENTANYL TRANSDERMAL SYSTEM
FENTANYL TRANSDERMAL SYSTEM - 35356-639-05 - (fentanyl transdermal system)
Drug Information of FENTANYL TRANSDERMAL SYSTEM
| Product NDC: | 35356-639 |
| Proprietary Name: | FENTANYL TRANSDERMAL SYSTEM |
| Non Proprietary Name: | fentanyl transdermal system |
| Active Ingredient(s): | 100 ug/h & nbsp; fentanyl transdermal system |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FENTANYL TRANSDERMAL SYSTEM
| Product NDC: | 35356-639 |
| 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 Information of FENTANYL TRANSDERMAL SYSTEM
| Package NDC: | 35356-639-05 |
| Package Description: | 5 POUCH in 1 CARTON (35356-639-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
NDC Information of FENTANYL TRANSDERMAL SYSTEM
| NDC Code | 35356-639-05 |
| Proprietary Name | FENTANYL TRANSDERMAL SYSTEM |
| Package Description | 5 POUCH in 1 CARTON (35356-639-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
| Product NDC | 35356-639 |
| 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 | 100 |
| Strength Unit | ug/h |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
