NDC 68071-1887-01 - 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
- 68071-1887
- Requested NDC
- 68071-1887-01
- Package NDCs from labels
- 68071-1887-1, 68071-1887-5, 68071-1887-8, 68071-1887-4, 68071-1887-2, 68071-1887-3, 68071-1887-6, 68071-1887-9, 68071-1887-01
- Manufacturer
- NuCare Pharmaceuticals, Inc | NuCare Pharmaceuticals, Inc.
- Effective date
- 2024-07-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ZOLPIDEM TARTRATE - NuCare Pharmaceuticals, Inc | NuCare Pharmaceuticals, Inc. | NuCare Pharmaceuticals, Inc | NuCare Pharmaceuticals, Inc. | 2024-07-16 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-1887-1 | ZOLPIDEM TARTRATE | 10 in 1 BOTTLE | TABLET | 10 | 6 | |
| 68071-1887-2 | ZOLPIDEM TARTRATE | 20 in 1 BOTTLE | TABLET | 20 | 6 | |
| 68071-1887-3 | ZOLPIDEM TARTRATE | 30 in 1 BOTTLE | TABLET | 30 | 6 | |
| 68071-1887-4 | ZOLPIDEM TARTRATE | 14 in 1 BOTTLE | TABLET | 14 | 6 | |
| 68071-1887-5 | ZOLPIDEM TARTRATE | 15 in 1 BOTTLE | TABLET | 15 | 6 | |
| 68071-1887-6 | ZOLPIDEM TARTRATE | 60 in 1 BOTTLE | TABLET | 60 | 6 | |
| 68071-1887-8 | ZOLPIDEM TARTRATE | 28 in 1 BOTTLE | TABLET | 28 | 6 | |
| 68071-1887-9 | ZOLPIDEM TARTRATE | 90 in 1 BOTTLE | TABLET | 90 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68071-1887 | ZOLPIDEM TARTRATE TABLET [NUCARE PHARMACEUTICALS, INC] | 6 | Current NDC, Legacy NDC, 8 package rows | 20240717_4be6ce23-e7b1-510e-e054-00144ff8d46c.zip |
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 | Preferred Pharmaceuticals Inc. | 625fad5b-8817-4773-a2fc-20b662140e6e | 2025-10-08 | Boxed warning, Warnings, Adverse reactions | WY6W63843K |
| Powder | TITANIUM DIOXIDE | Oxygen Development LLC | 08b52f29-c1a0-c673-e063-6294a90a9a7a | 2025-09-05 | Warnings | 1K09F3G675 |
| Powder | TITANIUM DIOXIDE | Oxygen Development LLC | 08b8003f-40be-3380-e063-6294a90a4f6b | 2025-09-05 | Warnings | 1K09F3G675 |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | FSA Store Inc. | 3cd18f96-34f7-3f2c-e063-6294a90a3b7e | 2025-08-19 | Warnings | 1K09F3G675 |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Bryant Ranch Prepack | 028bf425-7a72-464d-a242-aa5deee1ac23 | 2025-08-08 | Boxed warning, Warnings, Adverse reactions | WY6W63843K |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | ST. MARY'S MEDICAL PARK PHARMACY | 3bc8a122-aa21-212c-e063-6394a90a3bda | 2025-08-07 | Boxed warning, Warnings, Adverse reactions | 854876 WY6W63843K |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Asclemed USA, Inc. | 9922ce14-b418-4235-9c59-d674a8e70210 | 2025-07-24 | Boxed warning, Warnings, Adverse reactions | 854876 854873 WY6W63843K |
| Ferrum rosatum Graphites | FERRUM ROSATUM GRAPHITES | Uriel Pharmacy Inc. | 1a4ca338-eada-4c0f-8bce-480244940c89 | 2025-06-27 | Warnings | 1K09F3G675 |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Aphena Pharma Solutions - Tennessee, LLC | 3882d72d-686b-406b-e063-6294a90a0b89 | 2025-06-26 | Boxed warning, Warnings, Adverse reactions | 854873 WY6W63843K |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Aphena Pharma Solutions - Tennessee, LLC | a1faca42-6e46-4586-97ac-050b724e7d2a | 2025-06-09 | Boxed warning, Warnings, Adverse reactions | WY6W63843K |
| Aquavit | AQUAVIT | Uriel Pharmacy Inc. | c1c0887a-c388-c737-e053-2a95a90a076c | 2025-06-06 | Warnings | 1K09F3G675 |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Proficient Rx LP | 92c58053-7ed8-4a3d-a2f7-8e30c4e5a367 | 2025-06-01 | Boxed warning, Warnings, Adverse reactions | 854876 854873 WY6W63843K |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Aphena Pharma Solutions - Tennessee, LLC | 349053e4-9885-ec0b-e063-6294a90ad79a | 2025-05-23 | Boxed warning, Warnings, Adverse reactions | 854876 WY6W63843K |
| Zolpidem | ZOLPIDEM TARTRATE | Aphena Pharma Solutions - Tennessee, LLC | 1e15d6e3-8d06-0936-e063-6394a90ab8db | 2025-05-22 | Boxed warning, Warnings, Adverse reactions | 854873 WY6W63843K |
| Powder | TITANIUM DIOXIDE | Oxygen Development LLC | 08b7eeeb-09ae-ffe6-e063-6294a90aba90 | 2025-05-07 | Warnings | 1K09F3G675 |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Advanced Rx of Tennessee, LLC | 3310d63e-d79a-175d-e063-6394a90a4270 | 2025-04-18 | Boxed warning, Warnings, Adverse reactions | 854876 WY6W63843K |
| Ambien | ZOLPIDEM TARTRATE | Sanofi-Aventis U.S. LLC | c36cadf4-65a4-4466-b409-c82020b42452 | 2025-04-15 | Boxed warning, Warnings, Adverse reactions | 854876 854873 WY6W63843K |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Asclemed USA, Inc. | 30c057fb-2e1b-4b9c-8c8a-79c322151e61 | 2025-04-11 | Boxed warning, Warnings, Adverse reactions | WY6W63843K |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Preferred Pharmaceuticals Inc. | d579c6ca-c820-49ff-92fb-2e6aaad3b052 | 2025-04-11 | Boxed warning, Warnings, Adverse reactions | 854876 WY6W63843K |
| RID Poison Ivy Rash Relief | CALAMINE AND ZINC OXIDE | Oystershell Consumer Health Inc. | 36c3af9a-2646-4427-e063-6394a90a2c5e | 2025-03-13 | Warnings | 1K09F3G675 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.