PHENYTOIN SODIUM
NDC 61919-815, PHENYTOIN SODIUM, capsule, from DIRECT RX.
- Product NDC
- 61919-815
- Status
- Listed
- Labeler
- DIRECT RX
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA040765
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/61919-815 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENYTOIN SODIUM100 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]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 61919-815-30 | 61919081530 | 30 CAPSULE in 1 BOTTLE (61919-815-30) |
| 61919-815-71 | 61919081571 | 100 CAPSULE in 1 BOTTLE (61919-815-71) |
| 61919-815-72 | 61919081572 | 120 CAPSULE in 1 BOTTLE (61919-815-72) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/df0bf42b-ce9a-42c3-8c24-46f1ea3bd214
Use it
Look up 61919-815 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/61919-815 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 61919-815. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.