NDC 53489-600-06 - ZOLPIDEM TARTRATE
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 53489-600
- Requested NDC
- 53489-600-06
- Package NDCs from labels
- 53489-600-07, 53489-600-06, 53489-600-01, 53489-600-03, 53489-600-05, 53489-600-10
- Manufacturer
- Mutual Pharmaceutical Company, Inc.
- Effective date
- 2007-05-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ZOLPIDEM TARTRATE - Mutual Pharmaceutical Company, Inc. | Mutual Pharmaceutical Company, Inc. | 2007-05-04 | HUMAN PRESCRIPTION DRUG LABEL WITH HIGHLIGHTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53489-600-01 | ZOLPIDEM TARTRATE | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 1 | |
| 53489-600-03 | ZOLPIDEM TARTRATE | 250 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 250 | 1 | |
| 53489-600-05 | ZOLPIDEM TARTRATE | 500 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 500 | 1 | |
| 53489-600-06 | ZOLPIDEM TARTRATE | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | 1 | |
| 53489-600-07 | ZOLPIDEM TARTRATE | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | 1 | |
| 53489-600-10 | ZOLPIDEM TARTRATE | 1000 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1000 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Aphena Pharma Solutions - Tennessee, LLC | 7abb6898-223c-487b-856c-068ac04f7a5c | 2018-09-25 | Warnings, Adverse reactions | 854876 854873 |
| D86118D8-D3D0-6F36-2DA8-18B77607F8A5 | A0E521C3-7807-464E-922D-CE8F23216828 | 2007-05-04 | Warnings, Adverse reactions | D86118D8-D3D0-6F36-2DA8-18B77607F8A5 A0E521C3-7807-464E-922D-CE8F23216828 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.