63323-715Level 3
Fulvestrant (Fulvestrant)
**Product type:** Human Prescription Drug
**Active ingredient:** FULVESTRANT
**Strength:** 50 mg/mL
**Dosage form:** Injection, Solution
**Route:** Intramuscular
**Labeler:** Fresenius Kabi USA, LLC
**Marketing category:** NDA (NDA210326)
**Pharmacologic class:** Estrogen Receptor Antagonist [EPC], Estrogen Receptor Antagonists [MoA], Selective Estrogen Receptor Modulators [MoA]
GET
/api/v1/systems/ndc_fda/nodes/63323-715Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.