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Tretinoin

NDC 59651-712, Tretinoin, gel, from Aurobindo Pharma Limited.

Product NDC
59651-712
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218246
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-712 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRETINOIN.1 mg/g

Pharmacologic classes

Retinoid [EPC]; Retinoids [CS]

Package NDCNDC-11Package
59651-712-14596510712141 TUBE in 1 CARTON (59651-712-14) / 15 g in 1 TUBE
59651-712-46596510712461 TUBE in 1 CARTON (59651-712-46) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f64e45d7-bbc0-4da4-9ccb-e3941f22fdbe

  • NADAC price for package 59651071214

    GET /v1/drugs/nadac/59651071214

  • NADAC price for package 59651071246

    GET /v1/drugs/nadac/59651071246

Use it

Look up 59651-712 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-712 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-712. 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.