NDC 70756-850 – Naloxone hydrochloride
Naloxone Hydrochloride .4 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous
Product NDC70756-850
Product details
- Brand name
- Naloxone hydrochloride
- Generic name
- Naloxone hydrochloride
- Labeler
- Lifestar Pharma LLC
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA218404
- Marketed since
- February 19, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist
Active ingredients
- Naloxone Hydrochloride .4 mg/mL
Uses, dosage, side effects and warnings for Naloxone Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70756-850-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (70756-850-10) / 1 mL in 1 VIAL, SINGLE-DOSE | Feb 19, 2026 |
| 70756-850-25 | 25 VIAL, SINGLE-DOSE in 1 CARTON (70756-850-25) / 1 mL in 1 VIAL, SINGLE-DOSE | Feb 19, 2026 |
| 70756-850-82 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70756-850-82) / 1 mL in 1 VIAL, SINGLE-DOSE | Feb 19, 2026 |
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