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Terbinafine

NDC 16714-795, Terbinafine Hydrochloride, tablet, from NorthStar Rx LLC.

Product NDC
16714-795
Status
Listed
Labeler
NorthStar Rx LLC
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/16714-795 \
  -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
16714-795-011671407950130 TABLET in 1 BOTTLE (16714-795-01)
16714-795-0216714079502100 TABLET in 1 BOTTLE (16714-795-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8f87e3e1-4c9c-497a-af20-8ab52cfeef60

  • NADAC price for package 16714079501

    GET /v1/drugs/nadac/16714079501

  • NADAC price for package 16714079502

    GET /v1/drugs/nadac/16714079502

Use it

Look up 16714-795 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-795 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-795. 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.