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Tretinoin

NDC 72162-1220, Tretinoin, capsule, from Bryant Ranch Prepack.

Product NDC
72162-1220
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201687
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1220 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRETINOIN10 mg/1

Pharmacologic classes

Retinoid [EPC]; Retinoids [CS]

Package NDCNDC-11Package
72162-1220-172162122001100 CAPSULE in 1 BOTTLE (72162-1220-1)
72162-1220-37216212200330 CAPSULE in 1 BOTTLE (72162-1220-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7a7974c7-8b6c-41ae-9a48-a08a1439087a

Use it

Look up 72162-1220 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1220 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1220. 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.