NDC 51662-1690 – Naloxone Hydrochloride
Naloxone Hydrochloride 1 mg/mL · Injection · Intramuscular, Intravenous, Subcutaneous
Product NDC51662-1690
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 · ANDA213209
- Marketed since
- March 18, 2020
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 51662-1690-3 | 10 POUCH in 1 CASE (51662-1690-3) / 1 BOX in 1 POUCH (51662-1690-2) / 1 SYRINGE in 1 BOX (51662-1690-1) / 2 mL in 1 SYRINGE | Mar 18, 2020 |
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