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Lidocaine

NDC 51672-3020, Lidocaine, ointment, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-3020
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
OINTMENT
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA086724
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-3020 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LIDOCAINE50 mg/g

Pharmacologic classes

Amide Local Anesthetic [EPC]; Amides [CS]; Antiarrhythmic [EPC]; Local Anesthesia [PE]

Package NDCNDC-11Package
51672-3020-2516723020021 TUBE in 1 CARTON (51672-3020-2) / 30 g in 1 TUBE
51672-3020-9516723020091 TUBE in 1 CARTON (51672-3020-9) / 35.44 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ae758020-a508-4a2e-8164-e6c324e826a3

  • NADAC price for package 51672302002

    GET /v1/drugs/nadac/51672302002

  • NADAC price for package 51672302009

    GET /v1/drugs/nadac/51672302009

Use it

Look up 51672-3020 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-3020 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-3020. 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.