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terbinafine hydrochloride

NDC 70518-3907, terbinafine hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-3907
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078163
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3907 \
  -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
70518-3907-17051839070130 TABLET in 1 BOTTLE, PLASTIC (70518-3907-1)
70518-3907-37051839070330 TABLET in 1 BLISTER PACK (70518-3907-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2886b2ff-815f-4621-bc28-1fea082c1920

Use it

Look up 70518-3907 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3907 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3907. 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.