NDC 51662-1239 – Naloxone Hydrochloride
Naloxone Hydrochloride 1 mg/mL · Injection · Parenteral
Product NDC51662-1239
Product details
- Brand name
- Naloxone Hydrochloride
- Generic name
- Naloxone Hydrochloride
- Labeler
- HF Acquisition Co. LLC, DBA HealthFirst
- Dosage form
- Injection
- Route
- Parenteral
- Marketing category
- ANDA · ANDA072076
- Marketed since
- September 3, 2018
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 51662-1239-1 | 1 SYRINGE, PLASTIC in 1 BOX (51662-1239-1) / 2 mL in 1 SYRINGE, PLASTIC | Sep 3, 2018 |
| 51662-1239-3 | 10 POUCH in 1 CASE (51662-1239-3) / 1 mL in 1 POUCH (51662-1239-2) | Oct 27, 2020 |
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