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Isotretinoin

NDC 57664-022, Isotretinoin, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-022
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021951
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-022 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ISOTRETINOIN25 mg/1

Pharmacologic classes

Retinoid [EPC]; Retinoids [CS]

Package NDCNDC-11Package
57664-022-97576640022973 BLISTER PACK in 1 BOX (57664-022-97) / 10 CAPSULE in 1 BLISTER PACK (57664-022-98)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b44200ba-6672-4ea7-b151-7caec3f53c9c

  • NADAC price for package 57664002297

    GET /v1/drugs/nadac/57664002297

Use it

Look up 57664-022 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-022 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-022. 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.