NDC 73377-081 - Sildenafil Citrate
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
- 73377-081
- Package NDCs from labels
- 73377-081-01, 73377-081-02, 73377-081-03, 73377-081-04
- Manufacturer
- AX Pharmaceutical Corp
- Effective date
- 2020-10-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sildenafil Citrate - AX Pharmaceutical Corp | AX Pharmaceutical Corp | 2020-10-28 | BULK INGREDIENT |
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 |
|---|---|---|---|---|---|---|
| Sildenafil | SILDENAFIL POWDER, | Camber Pharmaceuticals, Inc. | 598f2b9c-cfb9-4f26-8508-83ca5055c305 | 2024-03-13 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Chartwell RX, LLC | fcc9e04d-3507-4429-9ddd-c1fdee8acdbf | 2024-03-12 | Warnings, Adverse reactions | BW9B0ZE037 |
| sildenafil | SILDENAFIL | Virtus Pharmaceuticals, LLC | 8526e8f2-4bb4-430b-9e38-68ee68caa5a4 | 2024-01-30 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL CITRATE | ANI Pharmaceuticals, Inc. | 083da718-e934-4941-b083-a19b4ebe3935 | 2024-01-22 | Warnings, Adverse reactions | BW9B0ZE037 |
| sildenafil citrate | SILDENAFIL CITRATE | Novadoz Pharmaceuticals LLC | 18b327c1-19c9-4e33-ae02-de7cc900149c | 2024-01-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Proficient Rx LP | 88825206-1b91-4d95-876c-71100912d378 | 2024-01-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | Lupin Pharmaceuticals, Inc. | 407ee7fc-0022-4fac-9fa6-4285d774fdb3 | 2023-12-06 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | A-S Medication Solutions | bf1a22a2-6a69-46c9-933d-e474e88637e9 | 2023-11-24 | Warnings, Adverse reactions | BW9B0ZE037 |
| Viagra | SILDENAFIL CITRATE | Viatris Specialty LLC | d905dc8d-917f-4ea3-a4ee-a1ecf6967d4e | 2023-11-17 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | Aphena Pharma Solutions - Tennessee, LLC | cdab7ef5-39cb-45cc-b2bf-5f634f2f5499 | 2023-11-09 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Bryant Ranch Prepack | 7c01fd56-5dd6-4728-9f2a-e0f5db810269 | 2023-10-30 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Proficient Rx LP | b9b1d6ee-da42-4ef2-ab93-cd36d7f34150 | 2023-10-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | Asclemed USA, Inc. | 49a95b25-08b3-4cfe-a60b-c5132c280be2 | 2023-09-13 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL CITRATE | ANI Pharmaceuticals, Inc. | 6d8dbaa6-d61a-46ae-a641-f664104f4714 | 2023-09-05 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Macleods Pharmaceuticals Limited | d2892f4b-f5ba-42f5-b373-310241f4efa7 | 2023-08-11 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | A-S Medication Solutions | 997197bf-7706-4e12-97df-b0a9ea6d3a10 | 2023-07-28 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Asclemed USA, Inc. | 0500a861-359f-4e12-beb5-0cac8cd6ae1c | 2023-05-10 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | CIPLA USA INC., | 15372a7c-2935-48dc-a55a-8966719b50be | 2023-05-02 | Warnings, Adverse reactions | BW9B0ZE037 |
| Revatio | SILDENAFIL CITRATE | PFIZER LABORATORIES DIV PFIZER INC | f158fe10-d5dc-4432-b2c9-fc665401291b | 2023-01-27 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | XLCARE Pharmaceuticals INC. | ae732301-384f-43ae-80d1-5e3784fe1dca | 2023-01-17 | Warnings, Adverse reactions | BW9B0ZE037 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.