Fentanyl Transdermal 00406-9175
Product NDC
00406-9175- Manufacturer
- Specgx Llc
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- May 6, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA077154
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fentanyl | 75 ug/h |
Drug Class
Opioid Agonist [EPC]Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
5 POUCH in 1 CARTON (0406-9175-76) / 1 PATCH in 1 POUCH / 72 h in 1 PATCH