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Lidocaine

NDC 51672-3008, Lidocaine, ointment, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-3008
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/51672-3008 \
  -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
51672-3008-5516723008051 JAR in 1 CARTON (51672-3008-5) / 50 g in 1 JAR

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5eb2c62f-5352-41d7-bd66-c65b1988a9ab

  • NADAC price for package 51672300805

    GET /v1/drugs/nadac/51672300805

Use it

Look up 51672-3008 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-3008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-3008. 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.