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Fentanyl - NOVAPLUS
Fentanyl - NOVAPLUS - 0591-3601-72 - (Fentanyl)
Drug Information of Fentanyl - NOVAPLUS
| Product NDC: | 0591-3601 |
| Proprietary Name: | Fentanyl - NOVAPLUS |
| Non Proprietary Name: | Fentanyl |
| Active Ingredient(s): | 50 ug/h & nbsp; Fentanyl |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fentanyl - NOVAPLUS
| Product NDC: | 0591-3601 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076709 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070901 |
Package Information of Fentanyl - NOVAPLUS
| Package NDC: | 0591-3601-72 |
| Package Description: | 5 POUCH in 1 CARTON (0591-3601-72) > 1 PATCH in 1 POUCH (0591-3601-54) > 72 h in 1 PATCH |
NDC Information of Fentanyl - NOVAPLUS
| NDC Code | 0591-3601-72 |
| Proprietary Name | Fentanyl - NOVAPLUS |
| Package Description | 5 POUCH in 1 CARTON (0591-3601-72) > 1 PATCH in 1 POUCH (0591-3601-54) > 72 h in 1 PATCH |
| Product NDC | 0591-3601 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fentanyl |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20070901 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | FENTANYL |
| Strength Number | 50 |
| Strength Unit | ug/h |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
