NDC 53489-286 - 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
- 53489-286
- Package NDCs from labels
- 53489-286-07, 53489-286-06, 53489-286-01, 53489-286-03, 53489-286-05, 53489-286-10
- Manufacturer
- MUTUAL PHARMACEUTICAL COMPANY, INC.
- Effective date
- 2007-01-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| GABAPENTIN CAPSULES | MUTUAL PHARMACEUTICAL COMPANY, INC. | 2007-01-17 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53489-286-01 | Gabapentin | 100 in 1 BOTTLE, PLASTIC | CAPSULE | 100 | 1 | |
| 53489-286-03 | Gabapentin | 250 in 1 BOTTLE, PLASTIC | CAPSULE | 250 | 1 | |
| 53489-286-05 | Gabapentin | 500 in 1 BOTTLE, PLASTIC | CAPSULE | 500 | 1 | |
| 53489-286-06 | Gabapentin | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | 1 | |
| 53489-286-07 | Gabapentin | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | 1 | |
| 53489-286-10 | Gabapentin | 1000 in 1 BOTTLE, PLASTIC | CAPSULE | 1000 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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 | Proficient Rx LP | 4bae5032-f634-4d1e-b672-8a7e2bd6a5fa | 2019-11-01 | Warnings, Adverse reactions | 310430 |
| GABAPENTIN | GABAPENTIN | Proficient Rx LP | 92c4d589-533b-4fe4-833f-dd68cc1f7e66 | 2019-11-01 | Warnings, Adverse reactions | 310432 |
| Gabapentin | GABAPENTIN | Proficient Rx LP | 2ef99c3d-866a-438b-a340-8beba8d4c457 | 2019-11-01 | Warnings, Adverse reactions | 310431 |
| Gabapentin | GABAPENTIN | Epic Pharma, LLC | 030e656a-e384-49ac-830f-32140c18112d | 2019-01-07 | Warnings, Adverse reactions | 310430 310432 310431 |
| GABAPENTIN | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | a900bafb-8f49-4a01-ba7f-4fb228ec0253 | 2018-11-12 | Warnings, Adverse reactions | 310431 |
| GABAPENTIN | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 6702ed8f-4aaf-46fa-bf39-db75154aa44c | 2018-10-19 | Warnings, Adverse reactions | 310432 |
| Gabapentin | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 1b73e9db-eddb-49ba-9778-01d39ece4d16 | 2018-09-21 | Warnings, Adverse reactions | 310431 |
| Gabapentin | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | f455b415-12a2-4916-b826-246976a8af44 | 2018-09-12 | Warnings, Adverse reactions | 310431 |
| Gabapentin | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 5fbd601f-df95-4a79-a7d3-c3505e23b913 | 2018-09-06 | Warnings, Adverse reactions | 310430 |
| GABAPENTIN | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 9d1b9121-c25a-4d28-91c5-5fc72f1167f4 | 2018-07-12 | 310431 | |
| Gabapentin | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 37d4d465-19a5-46db-80dc-0b7334b3343a | 2018-06-25 | Warnings, Adverse reactions | 310430 |
| Gabapentin | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 6fc8e8b2-5d0e-4c72-9a46-6d312c3efac7 | 2018-05-14 | Warnings, Adverse reactions | 310432 |
| Gabapentin | GABAPENTIN | Aphena Pharma Solutions - Tennessee, LLC | 86b30e64-fe56-42b3-a0f8-d9ef5d4b8c49 | 2016-06-20 | Warnings, Adverse reactions | 310432 310431 |
| Gabapentin | GABAPENTIN | Bi-Coastal Pharma International LLC | e0cd96d1-b1ef-46ec-a5a3-9505b0811b8b | 2016-04-17 | Warnings, Adverse reactions | 310430 310432 310431 |
| A36432F9-BDDD-4B22-BE6D-ED6AC2B3846A | A36432F9-BDDD-4B22-BE6D-ED6AC2B3846A | 2007-01-17 | Warnings, Adverse reactions | A36432F9-BDDD-4B22-BE6D-ED6AC2B3846A A36432F9-BDDD-4B22-BE6D-ED6AC2B3846A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.