FENTANYL TRANSDERMAL
- Product NDC
- 0406-9075
- 11-digit product format
- 004069075
- Labeler code
- 0406
- Product ID
- 0406-9075_301a8c6d-a664-4eac-9c9e-8c47eb34dae4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fentanyl transdermal
- Dosage form
- PATCH, EXTENDED RELEASE
- Route
- TRANSDERMAL
- Labeler
- SpecGx LLC
- Application
- ANDA077154
- Marketing category
- ANDA
- Marketing start
- 2011-02-09
- Marketing end
- 0000-00-00
- Substance
- FENTANYL
- Active strength
- 75 ug/h
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0406-9075-76 | 00406907576 | 5 POUCH in 1 CARTON (0406-9075-76) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH | 5 pouch | 2011-02-09 | 0000-00-00 | No | No | Current |