NDC 68071-3686-01 - DIAZEPAM
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
- 68071-3686
- Requested NDC
- 68071-3686-01
- Package NDCs from labels
- 68071-3686-3, 68071-3686-1, 68071-3686-01
- Manufacturer
- NuCare Pharmaceuticals, Inc
- Effective date
- 2024-10-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DIAZEPAM - NuCare Pharmaceuticals, Inc | NuCare Pharmaceuticals, Inc | 2024-10-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-3686-1 | DIAZEPAM | 10 in 1 BOTTLE | TABLET | 10 | 2 | |
| 68071-3686-3 | DIAZEPAM | 30 in 1 BOTTLE | TABLET | 30 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68071-3686 | DIAZEPAM TABLET [NUCARE PHARMACEUTICALS, INC] | 2 | Current NDC, 2 package rows | 20241010_22688087-27ad-620c-e063-6394a90a134c.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 |
|---|---|---|---|---|---|---|
| DIAZEPAM | DIAZEPAM | Henry Schein, Inc. | 52fc91f4-992f-47cb-a7d2-b26d74577481 | 2026-03-24 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | REMEDYREPACK INC. | d7a4b3c7-7021-4764-8c21-49e4bc6f6058 | 2026-03-12 | Boxed warning, Warnings, Adverse reactions | 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Safecor Health, LLC | 8b51f4b3-a5e8-4400-b624-ac0c47630c86 | 2026-02-20 | Boxed warning, Warnings, Adverse reactions | 197591 197590 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Henry Schein, Inc. | bfa85a63-967f-4176-a752-0bafabbaaae3 | 2026-02-19 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Natco Pharma USA LLC | 6b8dc373-fa01-42c9-89af-4e00bf00180a | 2026-02-12 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Sagent Pharmaceuticals | 7a912f1a-deee-46df-a8df-22a0afb06529 | 2026-02-04 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Direct_Rx | 181cc7ac-5129-2200-e063-6394a90afd3a | 2026-01-20 | Boxed warning, Warnings, Adverse reactions | 197589 Q3JTX2Q7TU |
| Lotrimin Daily Sweat and Odor Control | TOPICAL STARCH | Bayer HealthCare LLC. | 9ec5c80d-b550-496f-e053-2a95a90a5489 | 2026-01-16 | Warnings | O8232NY3SJ |
| DIAZEPAM | DIAZEPAM | Direct_Rx | 4b0c9c0a-4274-4d56-a7a4-bc497916469c | 2026-01-08 | Warnings, Adverse reactions | 197591 197589 Q3JTX2Q7TU |
| Medicated Cornstarch Baby Powder | ACTIVE CORN STARCH | Davion, Inc. | e39032d1-c8cd-4a41-af10-126970b8ad38 | 2025-12-29 | Warnings | O8232NY3SJ |
| Diazepam | DIAZEPAM | Lupin Pharmaceuticals,Inc. | d99b68aa-b3dc-49c8-8894-3da255cd26b0 | 2025-12-10 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM ORAL | Chartwell RX, LLC | cdb839fb-27e5-4a11-aed6-da0a7ab6e996 | 2025-12-03 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Valium | DIAZEPAM | Roche Laboratories Inc. | 554baee5-b171-4452-a50a-41a0946f956c | 2025-12-01 | Boxed warning, Warnings, Adverse reactions | 197591 197590 Q3JTX2Q7TU |
| DIAZEPAM | DIAZEPAM | Henry Schein, Inc. | dcf7bc20-6c57-491a-b9e3-f42bacff8b99 | 2025-11-18 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM ORAL | Chartwell Governmental & Specialty RX, LLC. | 167ee280-be68-4a28-a7d8-de41df14bc48 | 2025-11-10 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| DIAZEPAM | DIAZEPAM | ASCLEMED USA INC. | 426f3da1-4105-ba0a-e063-6294a90a7a86 | 2025-10-31 | Boxed warning, Warnings, Adverse reactions | ANDA217843 197591 197590 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | A-S Medication Solutions | 01f04ee4-fff9-499a-8213-984e16368084 | 2025-10-27 | Boxed warning, Warnings, Adverse reactions | 197590 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | PD-Rx Pharmaceuticals, Inc. | c2768add-5e01-4ff4-afa3-230380d59a1f | 2025-10-20 | Boxed warning, Warnings, Adverse reactions | 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | PD-Rx Pharmaceuticals, Inc. | 1ad84940-40f7-457a-8ffa-53e1a7bfee16 | 2025-10-17 | Boxed warning, Warnings, Adverse reactions | 197590 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | PD-Rx Pharmaceuticals, Inc. | 2483426d-3782-432a-8b8d-86c06ef0de4a | 2025-10-17 | Boxed warning, Warnings, Adverse reactions | 197591 Q3JTX2Q7TU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.