84571-140Level 3
ZIMHI (Naloxone Hydrochloride)
**Product type:** Human Prescription Drug
**Active ingredient:** NALOXONE HYDROCHLORIDE
**Strength:** 5 mg/.5mL
**Dosage form:** Injection, Solution
**Route:** Intramuscular; Subcutaneous
**Labeler:** ZMI Pharma Inc.
**Marketing category:** NDA (NDA212854)
**Pharmacologic class:** Opioid Antagonist [EPC], Opioid Antagonists [MoA]
GET
/api/v1/systems/ndc_fda/nodes/84571-140Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.