NDC 70069-672 – Nalbuphine hydrochloride
Nalbuphine Hydrochloride 20 mg/mL · Injection · Intramuscular, Intravenous, Subcutaneous
Product NDC70069-672
Product details
- Brand name
- Nalbuphine hydrochloride
- Generic name
- Nalbuphine hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- Injection
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA216050
- Marketed since
- September 25, 2024
- 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 |
|---|---|---|
| 70069-672-10 | 10 AMPULE in 1 CARTON (70069-672-10) / 1 mL in 1 AMPULE (70069-672-01) | Sep 25, 2024 |
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