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TERBINAFINE

NDC 87564-010, terbinafine hydrochloride tablet, tablet, from Amerisyn LLC.

Product NDC
87564-010
Status
Listed
Labeler
Amerisyn LLC
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/87564-010 \
  -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
87564-010-1087564001010100 TABLET in 1 BOTTLE (87564-010-10)
87564-010-308756400103030 TABLET in 1 BOTTLE (87564-010-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/584d1fae-0120-49a0-e063-6394a90a36fc

Use it

Look up 87564-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87564-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87564-010. 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.