Fentanyl Citrate
- Product NDC
- 0409-1276
- 11-digit product format
- 004091276
- Labeler code
- 0409
- Product ID
- 0409-1276_a7fc0d6b-ea67-43f2-b6ad-912d69a8781c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENTANYL CITRATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA072786
- Marketing category
- ANDA
- Marketing start
- 2005-07-20
- Marketing end
- 0000-00-00
- Substance
- FENTANYL CITRATE
- Active strength
- 50 ug/mL
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0409-1276-32 | 00409127632 | 10 CARTRIDGE in 1 CARTON (0409-1276-32) > 2 mL in 1 CARTRIDGE (0409-1276-03) | 10 cartridge | 2005-07-20 | 0000-00-00 | No | No | Current |