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Metronidazole

NDC 51672-4164, Metronidazole, gel, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4164
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204651
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4164 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METRONIDAZOLE10 mg/g

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC]; Nitroimidazoles [CS]

Package NDCNDC-11Package
51672-4164-3516724164031 TUBE in 1 CARTON (51672-4164-3) / 60 g in 1 TUBE
51672-4164-6516724164061 TUBE in 1 CARTON (51672-4164-6) / 45 g in 1 TUBE
51672-4164-9516724164091 BOTTLE, PUMP in 1 CARTON (51672-4164-9) / 55 g in 1 BOTTLE, PUMP

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a504f74-bccd-433a-bd5b-6822f98c34df

Use it

Look up 51672-4164 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4164 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4164. 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.