Ambien
NDC 0024-5401, zolpidem tartrate, tablet, film coated, from Sanofi-Aventis U.S. LLC.
- Product NDC
- 0024-5401
- Status
- Listed
- Labeler
- Sanofi-Aventis U.S. LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA019908
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/0024-5401 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ZOLPIDEM TARTRATE5 mg/1
Pharmacologic classes
Central Nervous System Depression [PE]; GABA A Receptor Positive Modulators [MoA]; gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0024-5401-31 | 00024540131 | 100 TABLET, FILM COATED in 1 BOTTLE (0024-5401-31) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c36cadf4-65a4-4466-b409-c82020b42452
Use it
Look up 0024-5401 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0024-5401 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0024-5401. 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.