NDC 42192-614 – Phenytoin Sodium

Phenytoin Sodium 50 mg/mL · Injection · Intramuscular, Intravenous

Human Prescription Drug 2 recalls

Product NDC42192-614

Product details

Brand name
Phenytoin Sodium
Generic name
Phenytoin Sodium
Labeler
Acella Pharmaceuticals, LLC
Dosage form
Injection
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA040573
Marketed since
December 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Phenytoin Sodium →

Package NDC codes (2)

Package NDCDescriptionSince
42192-614-1010 VIAL in 1 CARTON (42192-614-10) / 2 mL in 1 VIALDec 30, 2021
42192-614-3010 VIAL in 1 CARTON (42192-614-30) / 5 mL in 1 VIALDec 30, 2021

Recalls mentioning this NDC

Other Phenytoin Sodium products