NDC 69238-2348-01 - Tramadol 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
- 69238-2348
- Requested NDC
- 69238-2348-01
- Package NDCs from labels
- 69238-2348-4, 69238-2348-1, 69238-2348-5, 69238-2348-7, 69238-2348-01
- Manufacturer
- Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals, LLC
- Effective date
- 2026-01-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TRAMADOL - Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals, LLC | Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals, LLC | 2026-01-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69238-2348-1 | Tramadol Hydrochloride | 100 in 1 BOTTLE | TABLET, COATED | 100 | 51 | |
| 69238-2348-4 | Tramadol Hydrochloride | 10 in 1 BOTTLE | TABLET, COATED | 10 | 51 | |
| 69238-2348-5 | Tramadol Hydrochloride | 500 in 1 BOTTLE | TABLET, COATED | 500 | 51 | |
| 69238-2348-7 | Tramadol Hydrochloride | 1000 in 1 BOTTLE | TABLET, COATED | 1000 | 51 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69238-2348 | TRAMADOL HYDROCHLORIDE TABLET, COATED [AMNEAL PHARMACEUTICALS NY LLC] | 45 | Current NDC, Legacy NDC, 4 package rows | 20240215_67919c2c-2f8a-4bbb-bef5-0cd6c1e63a16.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.