NDC 62756-299 – Phenytoin sodium
Phenytoin Sodium 200 mg/1 · Capsule, Extended Release · Oral
Product NDC62756-299
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 · ANDA040731
- Marketed since
- June 30, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Phenytoin Sodium 200 mg/1
Uses, dosage, side effects and warnings for Phenytoin Sodium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 62756-299-08 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-08) | Jun 30, 2008 |
| 62756-299-13 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13) | Jun 30, 2008 |
| 62756-299-83 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-83) | Jun 30, 2008 |
| 62756-299-88 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-88) | Jun 30, 2008 |
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