NDC 81033-124-06 - Gabapentin
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
- 81033-124
- Requested NDC
- 81033-124-06
- Package NDCs from labels
- 81033-124-06, 81033-124-44
- Manufacturer
- Kesin Pharma Corporation
- Effective date
- 2025-09-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Gabapentin - Kesin Pharma Corporation | Kesin Pharma Corporation | 2025-09-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81033-124-06 | Gabapentin | 6 mL in 1 CUP, UNIT-DOSE | SOLUTION | 6 | 1 | |
| 81033-124-44 | Gabapentin | 40 in 1 CARTON | SOLUTION | 40 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 81033-124-06 | ML - Milliliter | 81033-124 | dac763c1-c481-43a1-86d4-7d259050a2c0 | 1 | 2025-10-14 |
| 81033-124-44 | ML - Milliliter | 81033-124 | 55a1fe8c-d9ba-4f1c-9663-d8638e8de22d | 1 | 2025-10-14 |
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 |
|---|---|---|---|---|---|---|
| Gabapentin | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 86b30e64-fe56-42b3-a0f8-d9ef5d4b8c49 | 2016-06-20 | Warnings, Adverse reactions | 6CW7F3G59X |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| Gabapentin | GABAPENTIN | Bi-Coastal Pharma International LLC | e0cd96d1-b1ef-46ec-a5a3-9505b0811b8b | 2016-04-17 | Warnings, Adverse reactions | 6CW7F3G59X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.