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Terbinafine Hydrochloride

NDC 55111-250, Terbinafine Hydrochloride, tablet, from Dr.Reddys Laboratories Limited.

Product NDC
55111-250
Status
Listed
Labeler
Dr.Reddys Laboratories Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076390
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-250 \
  -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
55111-250-0155111025001100 TABLET in 1 BOTTLE (55111-250-01)
55111-250-0555111025005500 TABLET in 1 BOTTLE (55111-250-05)
55111-250-305511102503030 TABLET in 1 BOTTLE (55111-250-30)
55111-250-795511102507910 BLISTER PACK in 1 CARTON (55111-250-79) / 10 TABLET in 1 BLISTER PACK (55111-250-78)
55111-250-905511102509090 TABLET in 1 BOTTLE (55111-250-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e0b309a5-bebe-c6da-2847-bda21aa488b1

Use it

Look up 55111-250 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-250. 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.