NDC 51672-4069 – Phenytoin
Phenytoin 125 mg/5mL · Suspension · Oral
Product NDC51672-4069
Product details
- Brand name
- Phenytoin
- Generic name
- Phenytoin
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA040521
- Marketed since
- April 8, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Phenytoin 125 mg/5mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4069-2 | 1 BOTTLE in 1 CARTON (51672-4069-2) / 237 mL in 1 BOTTLE | Jul 23, 2025 |
Recalls mentioning this NDC
- D-0863-2020 Mar 4, 2020 · Class I
Resuspension Problems: Two lots of Phenytoin Oral Suspension USP 125mg/5mL may coagulate and may not resuspend as per the label copy instructions.
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