Zolpidem Tartrate
- Product NDC
- 72789-390
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolpidem Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078413
- Marketing category
- ANDA
- Substance
- ZOLPIDEM TARTRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72789-390-21 | 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-390-21) | 2024-04-03 | | No | Historical |
| 72789-390-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-390-30) | 2024-04-03 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Zolpidem Tartrate | PD-Rx Pharmaceuticals, Inc. | 2025-01-30 | HUMAN PRESCRIPTION DRUG LABEL | 26 |