NDC 0409-1465 – Nalbuphine Hydrochloride
Nalbuphine Hydrochloride 20 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous
Product NDC0409-1465
Product details
- Brand name
- Nalbuphine Hydrochloride
- Generic name
- Nalbuphine Hydrochloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA070916
- Marketed since
- December 31, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist/Antagonist
Active ingredients
- Nalbuphine Hydrochloride 20 mg/mL
Uses, dosage, side effects and warnings for Nalbuphine hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0409-1465-01 | 10 AMPULE in 1 TRAY (0409-1465-01) / 1 mL in 1 AMPULE (0409-1465-71) | Dec 31, 2004 |
Recalls mentioning this NDC
- D-096-2013 Dec 26, 2012 · Class II
Lack of Assurance of Sterility: Complains of a loose crimp applied to the fliptop vial; and a missing stopper and flip cap were received and therefore sterility cannot be assured.
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