NDC 28595-705-01 - GONITRO
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
- 28595-705
- Requested NDC
- 28595-705-01
- Package NDCs from labels
- 28595-705-36, 28595-705-99, 28595-705-96, 28595-705-01, 28595-705-12
- Manufacturer
- Allegis Pharmaceuticals, Inc. | G. Pohl-Boskamp GmbH & Co. KG
- Effective date
- 2022-09-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| GONITRO - Allegis Pharmaceuticals, Inc. | G. Pohl-Boskamp GmbH & Co. KG | Allegis Pharmaceuticals, Inc. | G. Pohl-Boskamp GmbH & Co. KG | 2022-09-21 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 28595-705-01 | EA - Each | 28595-705 | ad094426-ebc9-4c39-b31a-31675718b9ef | 1 | 2020-06-05 |
| 28595-705-36 | EA - Each | 28595-705 | 6c56382c-8701-400e-a26c-03838b812ada | 1 | 2020-06-05 |
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 |
|---|---|---|---|---|---|---|
| Nitroglycerin In Dextrose | NITROGLYCERIN | Baxter Healthcare Company | 457a026c-ebce-4701-9deb-2d7652759a99 | 2016-08-22 | Warnings, Adverse reactions | G59M7S0WS3 |
| Eagle Brand Medicated Roll On Refresh | CAMPHOR, MENTHOL | Borden Company (Private) Limited | 567b6820-fb52-630e-e063-6294a90a8bf8 | 2015-07-01 | Warnings | AV092KU4JH |
| Nitroglycerin | NITROGLYCERIN | Mylan Pharmaceuticals Inc. | e98a2692-1cb9-4994-98d8-1d8d9ef1a256 | 2014-11-03 | Warnings, Adverse reactions | G59M7S0WS3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.