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Metronidazole

NDC 51672-4116, metronidazole, gel, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4116
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077819
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4116 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METRONIDAZOLE7.5 mg/g

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC]; Nitroimidazoles [CS]

Package NDCNDC-11Package
51672-4116-2516724116021 TUBE in 1 CARTON (51672-4116-2) / 30 g in 1 TUBE
51672-4116-5516724116055 g in 1 TUBE (51672-4116-5)
51672-4116-6516724116061 TUBE in 1 CARTON (51672-4116-6) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4a233572-2471-4e99-a45e-2de978abcf16
  • NADAC price for package 51672411606

    GET /v1/drugs/nadac/51672411606

Use it

Look up 51672-4116 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4116 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4116. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.