Phenytoin Sodium
- Product NDC
- 82804-269
- 11-digit product format
- 828040269
- Labeler code
- 82804
- Product ID
- 82804-269_f4353734-29b0-4027-824d-2fc97f778c67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenytoin Sodium
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040684
- Marketing category
- ANDA
- Marketing start
- 2006-09-05
- Substance
- PHENYTOIN SODIUM
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4182431BJH | PHENYTOIN SODIUM | 630-93-3 | PHENYTOIN SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-269-72 | 82804026972 | 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-269-72) | 2026-02-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Phenytoin Sodium | Proficient Rx LP | 2026-02-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |