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Terbinafine Hydrochloride

NDC 51991-526, Terbinafine Hydrochloride, tablet, from Breckenridge Pharmaceutical, Inc..

Product NDC
51991-526
Status
Listed
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077714
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51991-526 \
  -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
51991-526-0151991052601100 TABLET in 1 BOTTLE (51991-526-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c3832113-f517-4b4e-bf9c-31fce1a638e1

  • NADAC price for package 51991052601

    GET /v1/drugs/nadac/51991052601

Use it

Look up 51991-526 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51991-526 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51991-526. 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.