NDC 0143-9788 – Fosphenytoin Sodium
Fosphenytoin Sodium 50 mg/mL · Injection, Solution · Intramuscular, Intravenous
Product NDC0143-9788
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
- Fosphenytoin Sodium 50 mg/mL
Uses, dosage, side effects and warnings for Fosphenytoin Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9788-25 | 25 VIAL in 1 PACKAGE (0143-9788-25) / 2 mL in 1 VIAL (0143-9788-01) | Dec 2, 2009 |
Recalls mentioning this NDC
- D-1437-2012 Aug 8, 2012 · Class II
Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples. - D-1438-2012 Aug 8, 2012 · Class II
Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples.
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