NDC 70756-658 – naloxone hydrochloride

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

Human Prescription Drug

Product NDC70756-658

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 29, 2024
Listing expires
December 31, 2026
Pharmacologic class
Opioid Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70756-658-1010 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-10) / 1 mL in 1 VIAL, SINGLE-DOSEFeb 29, 2024
70756-658-2525 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-25) / 1 mL in 1 VIAL, SINGLE-DOSEFeb 29, 2024
70756-658-821 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-82) / 1 mL in 1 VIAL, SINGLE-DOSEFeb 29, 2024

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