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Miconazole Nitrate

NDC 51672-2070, Miconazole Nitrate, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-2070
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
VAGINAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076773
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2070 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MICONAZOLE NITRATE40 mg/g

Pharmacologic classes

Azole Antifungal [EPC]; Azoles [CS]

Package NDCNDC-11Package
51672-2070-9516722070091 TUBE, WITH APPLICATOR in 1 CARTON (51672-2070-9) / 25 g in 1 TUBE, WITH APPLICATOR

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 51672-2070 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2070 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-2070. 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.