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Tretinoin

NDC 51672-1407, tretinoin, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1407
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215713
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1407 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRETINOIN.25 mg/g

Pharmacologic classes

Retinoid [EPC]; Retinoids [CS]

Package NDCNDC-11Package
51672-1407-0516721407001 TUBE in 1 CARTON (51672-1407-0) / 20 g in 1 TUBE
51672-1407-9516721407091 TUBE in 1 CARTON (51672-1407-9) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2a31b13b-5cc8-4f6a-b364-872f6a478025

  • NADAC price for package 51672140700

    GET /v1/drugs/nadac/51672140700

  • NADAC price for package 51672140709

    GET /v1/drugs/nadac/51672140709

Use it

Look up 51672-1407 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1407 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1407. 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.