Zolpidem Tartrate
NDC 47335-308, Zolpidem Tartrate, tablet, film coated, extended release, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-308
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- 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/47335-308 \ -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 |
|---|---|---|
| 47335-308-13 | 47335030813 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-308-13) |
| 47335-308-88 | 47335030888 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-308-88) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/0c64bc71-2e7f-4b15-a8e1-acb8de04395fNADAC price for package 47335030888
GET /v1/drugs/nadac/47335030888
Use it
Look up 47335-308 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-308 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-308. 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.