NDC 0641-6132 – Naloxone Hydrochloride

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

Human Prescription Drug

Product NDC0641-6132

Product details

Brand name
Naloxone Hydrochloride
Generic name
Nalxone Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA070299
Marketed since
September 24, 1986
Listing expires
December 31, 2026
Pharmacologic class
Opioid Antagonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0641-6132-2525 VIAL in 1 CARTON (0641-6132-25) / 1 mL in 1 VIAL (0641-6132-01)Sep 24, 1986

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