Zolpidem Tartrate
NDC 71610-254, Zolpidem Tartrate, tablet, film coated, extended release, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-254
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204170
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/71610-254 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ZOLPIDEM TARTRATE12.5 mg/1
Pharmacologic classes
Central Nervous System Depression [PE]; GABA A Agonists [MoA]; Pyridines [CS]; gamma-Aminobutyric Acid-ergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71610-254-30 | 71610025430 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-254-30) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/ebd6c66b-b230-48d7-b38f-d610b6cb2b6c
Use it
Look up 71610-254 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-254 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-254. 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.