Phenytoin Sodium
NDC 70518-0107, Phenytoin Sodium, capsule, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-0107
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA040684
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0107 \ -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 |
|---|---|---|
| 70518-0107-0 | 70518010700 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-0107-0) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/e33ce05d-9c60-4ede-8b13-e8c41a3de25d
Use it
Look up 70518-0107 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0107 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-0107. 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.