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TERBINAFINE HYDROCHLORIDE

NDC 69292-225, Terbinafine Tablets 250 mg, tablet, from Amici Pharma, Inc..

Product NDC
69292-225
Status
Listed
Labeler
Amici Pharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076390
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69292-225 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TERBINAFINE HYDROCHLORIDE250 mg/1

Pharmacologic classes

Allylamine Antifungal [EPC]; Allylamine [CS]

Package NDCNDC-11Package
69292-225-0169292022501100 TABLET in 1 BOTTLE (69292-225-01)
69292-225-306929202253030 TABLET in 1 BOTTLE (69292-225-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd8724e9-bef9-4258-b536-9c6d872c3bf8

  • NADAC price for package 69292022501

    GET /v1/drugs/nadac/69292022501

  • NADAC price for package 69292022530

    GET /v1/drugs/nadac/69292022530

Use it

Look up 69292-225 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69292-225 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69292-225. 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.