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PHENYTOIN SODIUM

NDC 51662-1250, PHENYTOIN SODIUM, injection, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1250
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA084307
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1250 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENYTOIN SODIUM50 mg/mL

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
51662-1250-1516621250015 mL in 1 VIAL, SINGLE-DOSE (51662-1250-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/763b549d-9b78-09dd-e053-2a91aa0aec7f

Use it

Look up 51662-1250 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1250 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1250. 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.