NDC 70756-850 – Naloxone hydrochloride

Naloxone Hydrochloride .4 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug

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

Uses, dosage, side effects and warnings for Naloxone Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
70756-850-1010 VIAL, SINGLE-DOSE in 1 CARTON (70756-850-10) / 1 mL in 1 VIAL, SINGLE-DOSEFeb 19, 2026
70756-850-2525 VIAL, SINGLE-DOSE in 1 CARTON (70756-850-25) / 1 mL in 1 VIAL, SINGLE-DOSEFeb 19, 2026
70756-850-821 VIAL, SINGLE-DOSE in 1 CARTON (70756-850-82) / 1 mL in 1 VIAL, SINGLE-DOSEFeb 19, 2026

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