NDC 0143-9782 – Fosphenytoin Sodium

Fosphenytoin Sodium 50 mg/mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug 2 recalls

Product NDC0143-9782

Product details

Brand name
Fosphenytoin Sodium
Generic name
Fosphenytoin Sodium
Labeler
West-Ward Pharmaceuticals Corp
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA078765
Marketed since
December 2, 2009
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0143-9782-1010 VIAL in 1 PACKAGE (0143-9782-10) / 10 mL in 1 VIAL (0143-9782-01)Dec 2, 2009

Recalls mentioning this NDC

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