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Phenytoin

NDC 51672-4069, Phenytoin, suspension, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4069
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040521
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4069 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENYTOIN125 mg/5mL

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 NDCNDC-11Package
51672-4069-2516724069021 BOTTLE in 1 CARTON (51672-4069-2) / 237 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/093fd736-5971-47af-b4ef-08c1696cebe8

  • NADAC price for package 51672406902

    GET /v1/drugs/nadac/51672406902

Use it

Look up 51672-4069 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4069 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4069. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.