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DURAGESIC
DURAGESIC - 50458-090-05 - (fentanyl)
Drug Information of DURAGESIC
| Product NDC: | 50458-090 |
| Proprietary Name: | DURAGESIC |
| Non Proprietary Name: | fentanyl |
| Active Ingredient(s): | 12.5 ug/h & nbsp; fentanyl |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DURAGESIC
| Product NDC: | 50458-090 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019813 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900807 |
Package Information of DURAGESIC
| Package NDC: | 50458-090-05 |
| Package Description: | 5 POUCH in 1 BOX (50458-090-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
NDC Information of DURAGESIC
| NDC Code | 50458-090-05 |
| Proprietary Name | DURAGESIC |
| Package Description | 5 POUCH in 1 BOX (50458-090-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH |
| Product NDC | 50458-090 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fentanyl |
| Dosage Form Name | PATCH |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 19900807 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | FENTANYL |
| Strength Number | 12.5 |
| Strength Unit | ug/h |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
