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phenytoin sodium

NDC 62756-299, phenytoin sodium, capsule, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-299
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040731
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-299 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENYTOIN SODIUM200 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 NDCNDC-11Package
62756-299-0862756029908100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-08)
62756-299-1362756029913500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13)
62756-299-836275602998330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-83)
62756-299-8862756029988100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c40f66cc-6f4a-4b29-84ba-d265e4848735

Use it

Look up 62756-299 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-299 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-299. 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.