42192-614Level 3
PHENYTOIN SODIUM (PHENYTOIN SODIUM)
**Product type:** Human Prescription Drug
**Active ingredient:** PHENYTOIN SODIUM
**Strength:** 50 mg/mL
**Dosage form:** Injection
**Route:** Intramuscular; Intravenous
**Labeler:** Acella Pharmaceuticals, LLC
**Marketing category:** ANDA (ANDA040573)
**Pharmacologic class:** Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]
GET
/api/v1/systems/ndc_fda/nodes/42192-614Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.