Fentanyl - NOVAPLUS - Fentanyl
Navigation: NDC > Supplier starting with: W > WATSON LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-3601 |
| Proprietary Name: | Fentanyl - NOVAPLUS |
| Suffix: | |
| Non-Proprietary Name: | Fentanyl |
| Dosage Form: | PATCH, EXTENDED RELEASE |
| Method: | TRANSDERMAL |
| Original Marketing Date: | 01-09-2007 |
| Category Name: | ANDA |
| Application Number: | ANDA076709 |
| Labeler: | WATSON LABORATORIES, INC. |
| Substance Name: | FENTANYL |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | ug/h |
| Pharm Classes: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: | CII |