FENTANYL CITRATE
- Product NDC
- 0406-9206
- 11-digit product format
- 004069206
- Labeler code
- 0406
- Product ID
- 0406-9206_d96648d1-25f9-4a86-b771-55d298c5301b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENTANYL CITRATE
- Dosage form
- LOZENGE
- Route
- TRANSMUCOSAL
- Labeler
- SpecGx LLC
- Application
- ANDA078907
- Marketing category
- ANDA
- Marketing start
- 2009-10-30
- Marketing end
- 0000-00-00
- Substance
- FENTANYL CITRATE
- Active strength
- 600 ug/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0406-9206-30 | 00406920630 | 30 BLISTER PACK in 1 CARTON (0406-9206-30) > 1 LOZENGE in 1 BLISTER PACK | 30 blister pack | 2009-10-30 | 0000-00-00 | No | No | Current |