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Terbinafine

NDC 70518-4421, Terbinafine, tablet, from REMEDYREPACK INC..

Product NDC
70518-4421
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077533
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4421 \
  -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
70518-4421-07051844210090 TABLET in 1 BOTTLE, PLASTIC (70518-4421-0)
70518-4421-17051844210145 TABLET in 1 BOTTLE, PLASTIC (70518-4421-1)
70518-4421-27051844210230 TABLET in 1 BLISTER PACK (70518-4421-2)
70518-4421-37051844210330 TABLET in 1 BOTTLE, PLASTIC (70518-4421-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cacf5fe4-8c24-47ed-9a2b-b70aa5d45ef2

Use it

Look up 70518-4421 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4421 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4421. 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.