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 |
|---|---|---|---|---|---|---|
| Calamine | CALAMINE, PRAMOXIND HCL | Perrigo Direct, Inc | 54a20ec9-ab86-4410-af94-e04393e9d4b3 | 2026-02-19 | Warnings, Adverse reactions | 1K09F3G675 |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | NuCare Pharmaceuticals,Inc. | bca751bb-5161-5a95-e053-2a95a90aa2dd | 2026-02-19 | Boxed warning, Warnings, Adverse reactions | WY6W63843K |
| Calamine | CALAMINE, PRAMOXINE HCL | Meijer, Inc. | 6b369ef2-fd54-4931-a9eb-0fb42834c2ef | 2026-02-19 | Warnings, Adverse reactions | 1K09F3G675 |
| Calamine | FERRIC OXIDE RED | Target Corporation | d4ee05c8-ae62-45df-8783-1ed57fa030ec | 2026-02-18 | Warnings, Adverse reactions | 1K09F3G675 |
| Calamine | FERRIC OXIDE RED | Topco Associates LLC | 2b32e720-ac71-4d60-bc06-e28a00f8a450 | 2026-02-13 | Warnings, Adverse reactions | 1K09F3G675 |
| Calamine | CALAMINE, PRAMOXINE HCL | Topco Associates LLC | 15d1ae3f-509c-4e6b-8f0c-cf9265680358 | 2026-02-13 | Warnings, Adverse reactions | 1K09F3G675 |
| Calamine | FERRIC OXIDE RED | Major Pharmaceuticals | c25be68d-834a-4959-8d47-01ec789406ba | 2026-02-04 | Warnings, Adverse reactions | 1K09F3G675 |
| Aquavit 1 | AQUAVIT 1 | Uriel Pharmacy Inc. | 2354fcfc-05a2-444a-ace4-b3df61413157 | 2026-02-02 | Warnings | 1K09F3G675 |
| Calamine | CALAMINE | AMERISOURCE BERGEN | 90d9d908-57ea-4062-ade0-8a4888939c91 | 2026-01-29 | Warnings, Adverse reactions | 1K09F3G675 |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | A-S Medication Solutions | 2556c804-7a5e-4dbd-aeef-a3ba3a247c39 | 2026-01-23 | Boxed warning, Warnings, Adverse reactions | 854873 WY6W63843K |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | A-S Medication Solutions | f67ef513-1b2c-42fe-bf33-4c7e9db191a3 | 2026-01-22 | Boxed warning, Warnings, Adverse reactions | 854876 WY6W63843K |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Calvin Scott & Co., Inc. | 7da75d2b-905c-4fdf-bc53-1358c6477755 | 2026-01-15 | Boxed warning, Warnings, Adverse reactions | ANDA077903 854873 WY6W63843K |
| First Chakra (Root) 7301 | FIRST CHAKRA (ROOT) | Professional Complementary Health Formulas | 61eb1bbe-6675-4369-b852-18975e6b08c7 | 2026-01-08 | Warnings | 1K09F3G675 |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Direct_Rx | 907c7b18-2638-512c-e053-2995a90ae6fd | 2026-01-08 | Warnings, Adverse reactions | ANDA077903 854876 WY6W63843K |
| Third Chakra (Solar Plexus) 7303 | THIRD CHAKRA (SOLAR PLEXUS) | Professional Complementary Health Formulas | eea89c37-ab87-4cc7-8dfc-e7f42a580dd9 | 2026-01-08 | Warnings | 1K09F3G675 |
| Dermagesic | PRAMOXINE HCL, ZINC OXIDE, CALAMINE | Llorens Pharmaceutical International Division | bbff6b53-29da-45c1-8ccd-3e9df7f250e0 | 2025-12-31 | Warnings | 1K09F3G675 |
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Northwind Health Company, LLC | 47212207-52a1-938b-e063-6294a90abca8 | 2025-12-29 | Boxed warning, Warnings, Adverse reactions | 854873 WY6W63843K |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Northwind Health Company, LLC | 26e20f53-c042-eac0-e063-6394a90acfca | 2025-12-26 | Boxed warning, Warnings, Adverse reactions | ANDA077903 854873 WY6W63843K |
| ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | Lupin Pharmaceuticals, Inc. | ac647afe-2fe5-4056-806f-abdd54789b45 | 2025-12-26 | Boxed warning, Warnings, Adverse reactions | WY6W63843K |
| BABY ANTI MONKEY BUTT DIAPER RASH | ZINC OXIDE, CALAMINE | Clarion Brands, LLC | e4424d74-f89c-5943-42e8-bf3a38e68619 | 2025-12-23 | Warnings | 1K09F3G675 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.