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Terbinafine

NDC 65862-079, Terbinafine Hydrochloride, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-079
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078297
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-079 \
  -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
65862-079-0165862007901100 TABLET in 1 BOTTLE (65862-079-01)
65862-079-306586200793030 TABLET in 1 BOTTLE (65862-079-30)
65862-079-99658620079991000 TABLET in 1 BOTTLE (65862-079-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6600e2b3-65df-4fc3-8081-d574537d27e3

  • NADAC price for package 65862007930

    GET /v1/drugs/nadac/65862007930

Use it

Look up 65862-079 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-079 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-079. 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.