Zolpidem tartrate sublingual
NDC 49884-899, Zolpidem tartrate sublingual, tablet, from Par Health USA, LLC.
- Product NDC
- 49884-899
- Status
- Listed
- Labeler
- Par Health USA, LLC
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204229
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/49884-899 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ZOLPIDEM TARTRATE3.5 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 |
|---|---|---|
| 49884-899-11 | 49884089911 | 30 POUCH in 1 CARTON (49884-899-11) / 1 TABLET in 1 POUCH (49884-899-52) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/44b34e58-114b-4774-9fab-4b188dfe0228NADAC price for package 49884089911
GET /v1/drugs/nadac/49884089911
Use it
Look up 49884-899 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/49884-899 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 49884-899. 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.