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Terconazole

NDC 51672-1330, Terconazole, suppository, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1330
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SUPPOSITORY
Route
VAGINAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077553
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1330 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TERCONAZOLE80 mg/1

Pharmacologic classes

Azole Antifungal [EPC]; Azoles [CS]

Package NDCNDC-11Package
51672-1330-3516721330031 DOSE PACK in 1 CARTON (51672-1330-3) / 3 SUPPOSITORY in 1 DOSE PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b4f50a11-bd39-4023-9145-2da60f6b085f

Use it

Look up 51672-1330 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1330 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1330. 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.