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Tretinoin

NDC 71335-2952, Tretinoin, gel, from Bryant Ranch Prepack.

Product NDC
71335-2952
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA017955
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2952 \
  -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
71335-2952-1713352952011 TUBE in 1 CARTON (71335-2952-1) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/04f14d6e-5b44-44bd-a7f3-d684d9c5d7cb

Use it

Look up 71335-2952 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2952 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2952. 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.