NDC 42192-614 – Phenytoin Sodium
Phenytoin Sodium 50 mg/mL · Injection · Intramuscular, Intravenous
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
- Phenytoin Sodium 50 mg/mL
Uses, dosage, side effects and warnings for Phenytoin Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 42192-614-10 | 10 VIAL in 1 CARTON (42192-614-10) / 2 mL in 1 VIAL | Dec 30, 2021 |
| 42192-614-30 | 10 VIAL in 1 CARTON (42192-614-30) / 5 mL in 1 VIAL | Dec 30, 2021 |
Recalls mentioning this NDC
- D-0070-2023 Nov 30, 2022 · Class III
Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode. - D-0069-2023 Nov 30, 2022 · Class III
Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode.
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