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Tretinoin

NDC 68462-792, Tretinoin, capsule, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-792
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208279
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-792 \
  -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
68462-792-0168462079201100 CAPSULE in 1 BOTTLE (68462-792-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/264138c1-9e5f-45ef-be87-79ca97c989d9

  • NADAC price for package 68462079201

    GET /v1/drugs/nadac/68462079201

Use it

Look up 68462-792 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-792 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-792. 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.