0143-9392Level 3
REMIFENTANIL HYDROCHLORIDE (REMIFENTANIL HYDROCHLORIDE)
**Product type:** Human Prescription Drug
**Active ingredient:** REMIFENTANIL HYDROCHLORIDE
**Strength:** 2 mg/2mL
**Dosage form:** Injection, Powder, Lyophilized, For Solution
**Route:** Intravenous
**Labeler:** Hikma Pharmaceuticals USA Inc.
**Marketing category:** ANDA (ANDA210594)
**Pharmacologic class:** Full Opioid Agonists [MoA], Opioid Agonist [EPC]
**DEA schedule:** CII
GET
/api/v1/systems/ndc_fda/nodes/0143-9392Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.