67184-0501Level 3
Oxaliplatin (Oxaliplatin)
**Product type:** Human Prescription Drug
**Active ingredient:** OXALIPLATIN
**Strength:** 50 mg/10mL
**Dosage form:** Injection, Powder, Lyophilized, For Solution
**Route:** Intravenous
**Labeler:** Qilu Pharmaceutical Co., Ltd.
**Marketing category:** ANDA (ANDA204616)
**Pharmacologic class:** Platinum-based Drug [EPC], Platinum-containing Compounds [EXT]
GET
/api/v1/systems/ndc_fda/nodes/67184-0501Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.