NDC 51662-1671 – Naloxone Hydrochloride
Naloxone Hydrochloride .4 mg/mL · Injection · Intramuscular, Intravenous, Subcutaneous
Product NDC51662-1671
Product details
- Brand name
- Naloxone Hydrochloride
- Generic name
- Naloxone Hydrochloride
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Dosage form
- Injection
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA070299
- Marketed since
- September 24, 1986
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Antagonist
Active ingredients
- Naloxone Hydrochloride .4 mg/mL
Uses, dosage, side effects and warnings for Naloxone Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51662-1671-3 | 25 VIAL in 1 CARTON (51662-1671-3) / 1 mL in 1 VIAL (51662-1671-1) | Sep 24, 1986 |
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