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Terbinafine

NDC 71205-492, Terbinafine Hydrochloride, tablet, from Proficient Rx LP.

Product NDC
71205-492
Status
Listed
Labeler
Proficient Rx LP
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/71205-492 \
  -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
71205-492-307120504923030 TABLET in 1 BOTTLE (71205-492-30)
71205-492-357120504923535 TABLET in 1 BOTTLE (71205-492-35)
71205-492-427120504924242 TABLET in 1 BOTTLE (71205-492-42)
71205-492-457120504924545 TABLET in 1 BOTTLE (71205-492-45)
71205-492-607120504926060 TABLET in 1 BOTTLE (71205-492-60)
71205-492-907120504929090 TABLET in 1 BOTTLE (71205-492-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/50657431-1cd9-42dd-9cfc-57db8713d267

Use it

Look up 71205-492 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-492. 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.