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 | PD-Rx Pharmaceuticals, Inc. | 84cecab3-d0e6-436b-996b-0b598e972308 | 2025-10-17 | Boxed warning, Warnings, Adverse reactions | 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Natco Pharma USA LLC | 19d0e3e5-f081-4574-9f0a-e7e97a88c7a9 | 2025-09-08 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | A-S Medication Solutions | ec433be5-d84d-425f-9edf-71263f885eec | 2025-08-13 | Boxed warning, Warnings, Adverse reactions | 197590 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Precision Dose Inc. | 78d5a77d-5ca7-4f16-b4d0-fce86456593c | 2025-08-07 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Fresenius Kabi USA, LLC | ae52866a-0b9a-4baf-af1b-f9d5e00c0e56 | 2025-08-07 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Mylan Institutional Inc. | b326c66d-5762-4d16-933c-619fa2088ccd | 2025-07-18 | Boxed warning, Warnings, Adverse reactions | 197591 197590 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | A-S Medication Solutions | b47dc708-e83b-4224-bdb5-c9b7abd35cfb | 2025-06-09 | Boxed warning, Warnings, Adverse reactions | 197591 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Natco Pharma USA LLC | a14f5930-a3ac-4996-9778-df5baa3d0bab | 2025-04-24 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| DIAZEPAM | DIAZEPAM | Advanced Rx of Tennessee, LLC | 32c3af91-a57a-1278-e063-6294a90ae5ec | 2025-04-14 | Boxed warning, Warnings, Adverse reactions | ANDA217843 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Advanced Rx of Tennessee, LLC | 2d322c6a-7f7e-1cc4-e063-6294a90a8e2e | 2025-04-14 | Boxed warning, Warnings, Adverse reactions | 197591 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Civica, Inc. | 83646a0f-eb43-4871-b95e-683c2533d2be | 2025-04-07 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Asclemed USA, Inc. | 32e7bfa1-6060-4041-a0e5-249cacb84ebc | 2025-01-27 | Boxed warning, Warnings, Adverse reactions | 197591 197590 197589 Q3JTX2Q7TU |
| DIAZEPAM | DIAZEPAM | Proficient Rx LP | 9322b0bc-e9fa-4c89-808b-110decf6db58 | 2025-01-01 | Boxed warning, Warnings, Adverse reactions | ANDA217843 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Advanced Rx Pharmacy of Tennessee, LLC | b7002d26-3856-4c2f-e053-2995a90aea60 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 197589 Q3JTX2Q7TU |
| DIAZEPAM | DIAZEPAM | NuCare Pharmaceuticals, Inc. | 21785bb2-cc96-7973-e063-6294a90ab1b8 | 2024-12-26 | Boxed warning, Warnings, Adverse reactions | ANDA217843 197591 Q3JTX2Q7TU |
| DIAZEPAM | DIAZEPAM | Sunrise Pharmaceutical, Inc. | 34ac0b9d-d4ad-4aaa-8bee-902365f4e9a8 | 2024-12-09 | Boxed warning, Warnings, Adverse reactions | 197591 197590 197589 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Hikma Pharmaceuticals USA Inc. | 9e85abed-1a8b-4762-a31f-f2c7f196b8af | 2024-12-04 | Boxed warning, Warnings, Adverse reactions | Q3JTX2Q7TU |
| DIAZEPAM | DIAZEPAM | NuCare Pharmaceuticals, Inc | 22688087-27ad-620c-e063-6394a90a134c | 2024-10-08 | Boxed warning, Warnings, Adverse reactions | ANDA217843 68071-3686-1 68071-3686-3 68071-3686 68071368601 197591 23fdc250-87e3-f697-e063-6294a90a04dc 22688087-27ad-620c-e063-6394a90a134c Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Bryant Ranch Prepack | 9424ce71-f04c-4d70-89de-b7858931c53d | 2024-08-23 | Boxed warning, Warnings, Adverse reactions | 197591 Q3JTX2Q7TU |
| Diazepam | DIAZEPAM | Bryant Ranch Prepack | 632d7e96-d32c-45b8-86cf-f18ec2b35485 | 2024-08-23 | Boxed warning, Warnings, Adverse reactions | 197590 Q3JTX2Q7TU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.