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Terbinafine Hydrochloride

NDC 43063-906, Terbinafine Hydrochloride, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-906
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077714
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43063-906 \
  -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
43063-906-204306309062020 TABLET in 1 BOTTLE, PLASTIC (43063-906-20)
43063-906-424306309064242 TABLET in 1 BOTTLE, PLASTIC (43063-906-42)
43063-906-904306309069090 TABLET in 1 BOTTLE, PLASTIC (43063-906-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2df111dc-ecac-4161-9e22-38436eb37c1f

Use it

Look up 43063-906 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-906 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-906. 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.