Extended Phenytoin Sodium
NDC 70518-2227, Phenytoin Sodium, capsule, from REMEDYREPACK INC..
- Product NDC
- 70518-2227
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204309
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2227 \ -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 |
|---|---|---|
| 70518-2227-3 | 70518222703 | 30 CAPSULE in 1 BLISTER PACK (70518-2227-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/363cd347-d25e-42b9-9ce7-30642f3cb353
Use it
Look up 70518-2227 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2227 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2227. 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.