NDC 51672-4111 – Phenytoin Sodium
Phenytoin Sodium 100 mg/1 · Capsule, Extended Release · Oral
Product NDC51672-4111
Product details
- Brand name
- Phenytoin Sodium
- Generic name
- Phenytoin Sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA040684
- Marketed since
- September 5, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Phenytoin Sodium 100 mg/1
Uses, dosage, side effects and warnings for Phenytoin Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4111-1 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-1) | Sep 5, 2006 |
| 51672-4111-3 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-3) | Sep 5, 2006 |
| 51672-4111-6 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-6) | Sep 5, 2006 |
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