Isotretinoin
NDC 57664-024, Isotretinoin, capsule, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 57664-024
- 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
curl https://api.healthcare.dev/v1/drugs/ndc/57664-024 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ISOTRETINOIN35 mg/1
Pharmacologic classes
Retinoid [EPC]; Retinoids [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 57664-024-97 | 57664002497 | 3 BLISTER PACK in 1 BOX (57664-024-97) / 10 CAPSULE in 1 BLISTER PACK (57664-024-98) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b44200ba-6672-4ea7-b151-7caec3f53c9c
Use it
Look up 57664-024 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/57664-024 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 57664-024. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.