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terbinafine hydrochloride

NDC 82804-220, terbinafine hydrochloride, tablet, from Proficient Rx LP.

Product NDC
82804-220
Status
Listed
Labeler
Proficient Rx LP
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/82804-220 \
  -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
82804-220-308280402203030 TABLET in 1 BOTTLE, PLASTIC (82804-220-30)
82804-220-428280402204242 TABLET in 1 BOTTLE, PLASTIC (82804-220-42)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/53235270-6ffb-44c8-aa55-debf59e1d964

Use it

Look up 82804-220 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-220 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-220. 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.