NDC 80425-0296-01 - Venlafaxine hydrochloride ER
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
- 80425-0296
- Requested NDC
- 80425-0296-01
- Package NDCs from labels
- 80425-0296-1, 80425-0296-2, 80425-0296-3, 80425-0296-01
- Manufacturer
- Advanced Rx Pharmacy of Tennessee, LLC
- Effective date
- 2024-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Venlafaxine hydrochloride ER - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0296-1 | Venlafaxine hydrochlorideER | 30 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 30 | 2 | |
| 80425-0296-2 | Venlafaxine hydrochlorideER | 60 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 60 | 2 | |
| 80425-0296-3 | Venlafaxine hydrochlorideER | 90 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 90 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0296 | VENLAFAXINE HYDROCHLORIDE ER (VENLAFAXINE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 2 | Current NDC, 3 package rows | 20250102_f89bcae0-e714-599a-e053-6294a90a2c3a.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0296-1 | EA - Each | 80425-0296 | 19a8e1c7-fca1-48d6-905f-9e3760d8d660 | 1 | 2023-06-06 |
| 80425-0296-2 | EA - Each | 80425-0296 | 08f25694-74d0-4109-869d-0deeaaad811e | 1 | 2023-06-06 |
| 80425-0296-3 | EA - Each | 80425-0296 | c596b70e-071d-4424-9450-f764a0f86cf8 | 1 | 2023-06-06 |
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 |
|---|---|---|---|---|---|---|
| venlafaxine | VENLAFAXINE | Proficient Rx LP | cc3a1258-aafb-48cf-86f7-fcf59e0c6cdd | 2020-01-01 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| venlafaxine hydrochloride | VENLAFAXINE HYDROCHLORIDE | Dr.Reddy's Laboratories Ltd. | 7027be98-61d6-a986-c9df-60ceef5f7ff0 | 2018-12-06 | Boxed warning, Warnings, Adverse reactions | 313585 313583 313581 7D7RX5A8MO |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.