NDC 0409-1782 – Naloxone Hydrochloride

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

Human Prescription Drug 1 recall

Product NDC0409-1782

Product details

Brand name
Naloxone Hydrochloride
Generic name
Naloxone Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA070172
Marketed since
September 23, 2005
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
0409-1782-6910 CARTRIDGE in 1 BOX (0409-1782-69) / 1 mL in 1 CARTRIDGE (0409-1782-03)Sep 23, 2005

Recalls mentioning this NDC

Other Naloxone Hydrochloride products