NDC 76045-112 – Naloxone Hydrochloride
Naloxone Hydrochloride 1 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous
Product NDC76045-112
Product details
- Brand name
- Naloxone Hydrochloride
- Generic name
- Naloxone Hydrochloride
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA213573
- Marketed since
- April 2, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Antagonist
Active ingredients
- Naloxone Hydrochloride 1 mg/mL
Uses, dosage, side effects and warnings for Naloxone Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 76045-112-20 | 24 SYRINGE in 1 CASE (76045-112-20) / 2 mL in 1 SYRINGE (76045-112-01) | Apr 2, 2024 |
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