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terbinafine hydrochloride

NDC 69452-351, terbinafine hydrochloride, tablet, from Bionpharma Inc..

Product NDC
69452-351
Status
Listed
Labeler
Bionpharma Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078163
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69452-351 \
  -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
69452-351-136945203511330 TABLET in 1 BOTTLE, PLASTIC (69452-351-13)
69452-351-2069452035120100 TABLET in 1 BOTTLE, PLASTIC (69452-351-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/34221c17-0d8c-4b56-8af3-c74efab4599e

  • NADAC price for package 69452035113

    GET /v1/drugs/nadac/69452035113

  • NADAC price for package 69452035120

    GET /v1/drugs/nadac/69452035120

Use it

Look up 69452-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-351. 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.