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 | AvKARE | 21c83ff3-c359-3269-e063-6394a90a57ee | 2026-01-19 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Advagen Pharma Ltd | ce683bbc-a1d2-4f23-b3d1-d9333d91dc55 | 2026-01-13 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | Advagen Pharma Ltd | e671d887-2317-4c1c-9b68-e24cda3d3aef | 2026-01-07 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Northwind Health Company, LLC | fa14cb6b-0fa8-0ba0-e053-6294a90afae3 | 2026-01-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Northwind Health Company, LLC | f3089ee6-190d-4749-e053-2a95a90a15d8 | 2026-01-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Northwind Health Company, LLC | d9ddfd2a-1961-90f9-e053-2a95a90a7f9b | 2026-01-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | Northwind Health Company, LLC | d9de0817-cac1-4ee5-e053-2a95a90a5fa7 | 2026-01-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals, Inc. | 2916e6c4-bc68-c4d6-e063-6394a90aba79 | 2025-12-12 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | American Health Packaging | f7fbfc3b-807e-4375-a6eb-8db0eaf40c9c | 2025-11-20 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | AvPAK | e08de794-9b7e-aae6-9c89-a0c0d090cc76 | 2025-11-12 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Quallent Pharmaceuticals Health LLC | 333ca682-931f-4edb-95d6-2edbd87631cf | 2025-11-07 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Quallent Pharmaceuticals Health LLC | 41b67fd2-3d9a-49d6-88b8-285044b98dc1 | 2025-11-07 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Ajanta Pharma USA Inc. | 283790ed-2acb-4714-a0af-b348bb642785 | 2025-11-05 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | Proficient Rx LP | 8780c159-8b61-402b-afbe-64f5c85d3886 | 2025-11-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | Proficient Rx LP | 30ce6e7f-716e-4a68-a4fb-2bb2d34ed052 | 2025-11-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals,Inc. | 41b2c017-53a0-c687-e063-6394a90a15b2 | 2025-10-21 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Ajanta Pharma USA Inc. | 31c0f8ab-ed2e-4ead-a8c0-4055f6c43783 | 2025-10-09 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Ajanta Pharma USA Inc. | 2ccc6fa6-f8ae-4191-806f-a887244e516a | 2025-10-08 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Macleods Pharmaceuticals Limited | c2b25818-99a3-474b-a04c-929df1110834 | 2025-09-17 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Proficient Rx LP | 71140bd5-0a51-4c01-ad0d-193d08ea67dd | 2025-09-01 | Warnings, Adverse reactions | BW9B0ZE037 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.