Zolpidem Tartrate
NDC 80425-0060, Zolpidem Tartrate, tablet, coated, from Advanced Rx of Tennessee, LLC.
- Product NDC
- 80425-0060
- Status
- Listed
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077322
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0060 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ZOLPIDEM TARTRATE10 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 |
|---|---|---|
| 80425-0060-1 | 80425006001 | 30 TABLET, COATED in 1 BOTTLE (80425-0060-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/af87b722-cdb7-0b17-e053-2a95a90a315b
Use it
Look up 80425-0060 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0060 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80425-0060. 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.