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Phenytoin

NDC 0121-0892, Phenytoin, suspension, from PAI Holdings, LLC dba PAI Pharma.

Product NDC
0121-0892
Status
Listed
Labeler
PAI Holdings, LLC dba PAI Pharma
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/0121-0892 \
  -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
0121-0892-63001210892634 mL in 1 CUP, UNIT-DOSE (0121-0892-63)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2c74e35-ed8d-4ea6-b7a5-7be0b0155c15

Use it

Look up 0121-0892 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0892 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-0892. 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.