NDC 80425-0342-01 - Imipramine Hydrochloride
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
- 80425-0342
- Requested NDC
- 80425-0342-01
- Package NDCs from labels
- 80425-0342-1, 80425-0342-2, 80425-0342-3, 80425-0342-01
- 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 |
|---|---|---|---|
| Imipramine Hydrochloride - 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 |
|---|---|---|---|---|---|---|
| 80425-0342-1 | Imipramine Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 4 | |
| 80425-0342-2 | Imipramine Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 4 | |
| 80425-0342-3 | Imipramine Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0342 | IMIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 4 | Current NDC, 3 package rows | 20250102_fd78fb8e-99ae-91b0-e053-6394a90a9271.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0342-1 | EA - Each | 80425-0342 | dde2fdcb-29e6-40f6-b1e2-91340726269f | 1 | 2023-07-06 |
| 80425-0342-2 | EA - Each | 80425-0342 | a1752b69-50a9-4892-96b0-0ce0af54dca3 | 1 | 2023-07-06 |
| 80425-0342-3 | EA - Each | 80425-0342 | 3b7893e8-a32e-476d-b314-daff78ea3697 | 1 | 2023-07-06 |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.