ZOLPIDEM TARTRATE
NDC 70518-2917, zolpidem tartrate, tablet, from REMEDYREPACK INC..
- Product NDC
- 70518-2917
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077903
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2917 \ -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 |
|---|---|---|
| 70518-2917-1 | 70518291701 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2917-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2abdcf77-d3ed-42bc-acd9-545aab75d567
Use it
Look up 70518-2917 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2917 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2917. 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.