zolpidem tartrate
- Product NDC
- 51407-761
- 11-digit product format
- 514070761
- Labeler code
- 51407
- Product ID
- 51407-761_43faa293-f5ec-ef0b-e063-6294a90a755c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zolpidem tartrate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- NDA021774
- Marketing category
- NDA
- Marketing start
- 2005-09-02
- Substance
- ZOLPIDEM TARTRATE
- Active strength
- 6.25 mg/1
- Pharmacologic classes
- Central Nervous System Depression [PE], GABA A Receptor Positive Modulators [MoA], gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- zolpidem tartrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZOLPIDEM TARTRATE | 6.25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WY6W63843K |
| Rxcui | 854880, 854894 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-761-01 | zolpidem tartrate | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 51407-761-01 | 51407076101 | 100 TABLET, COATED in 1 BOTTLE (51407-761-01) | 2025-08-26 | No | No | Current |