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 | Proficient Rx LP | 7dd302cd-b84d-4d7d-bd1e-2916febbaea5 | 2025-08-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals,Inc. | d35f8d6b-e642-78bb-e053-2995a90abb2e | 2025-07-24 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Macleods Pharmaceuticals Limited | 61a0ebd9-8dc9-4bcc-b07b-f3d6398ea96e | 2025-06-21 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals, Inc. | 3314d14e-99eb-39e5-e063-6394a90aed94 | 2025-04-18 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | PD-Rx Pharmaceuticals, Inc. | dc4430cc-8238-4d6d-99ff-bbb9d0b51bd1 | 2025-04-04 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | Advanced Rx of Tennessee, LLC | 30cb7d6a-ce40-c794-e063-6294a90a6861 | 2025-03-20 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | NuCare Pharmaceuticals,Inc. | 155c7549-b7d6-0c06-e063-6294a90ac65c | 2025-03-17 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals,Inc. | f98d51a5-e3c8-2b6c-e053-6294a90ac146 | 2025-02-10 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Modavar Pharmaceuticals LLC | 8c4f22c8-3607-4d64-8821-dd3202f8fa0a | 2025-01-23 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Cadila Pharmaceuticals Limited | c079fc41-7b9a-499d-88ea-86ccb65c828d | 2025-01-23 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | DirectRx | d1ee9139-13ac-7d5b-e053-2995a90a8e50 | 2025-01-20 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | Preferred Pharmaceuticals Inc. | 5846bff2-6a93-46a7-a547-04459c590814 | 2025-01-20 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | DIRECT RX | a84a418a-155c-7be7-e053-2995a90a8158 | 2025-01-17 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals,Inc. | a9f0e832-e85c-975f-e053-2995a90afa22 | 2025-01-02 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | NuCare Pharmaceuticals, Inc. | 1d614710-708e-f11c-e063-6394a90a05a5 | 2024-12-26 | Warnings, Adverse reactions | BW9B0ZE037 |
| Revatio | SILDENAFIL CITRATE | Viatris Specialty LLC | 3bb9363e-b28d-4019-8aae-539233dca214 | 2024-12-18 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals, Inc. | 28f2af84-f4d4-acfe-e063-6294a90ae128 | 2024-12-10 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Bryant Ranch Prepack | 591a4ae7-e06c-42b6-85af-f03fd2fb8959 | 2024-11-20 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Bryant Ranch Prepack | f9ab796c-1912-4137-abec-e8336a850a58 | 2024-10-31 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | A-S Medication Solutions | 28a3376b-e50e-4789-9916-803ba29a1522 | 2024-10-25 | Warnings, Adverse reactions | BW9B0ZE037 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.