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 CITRATE | Eugia US LLC | bb92d686-a81e-4b91-8048-693af0534cb3 | 2026-07-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Bryant Ranch Prepack | 486dcfc4-f07a-4a78-86f0-f1c5ae448dc1 | 2026-06-29 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Bryant Ranch Prepack | e22902bd-e5a8-4df6-ae77-8a0a1484cc50 | 2026-06-29 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Northwind Health Company, LLC | 471b8574-cb2a-1670-e063-6394a90a2a84 | 2026-06-23 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Bryant Ranch Prepack | 824dcd79-bc82-4b3a-8028-3c1bca1a7a0a | 2026-06-18 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | PD-Rx Pharmaceuticals, Inc. | 4ca5555d-fd45-467b-8b1d-4fbe1404f1f3 | 2026-06-04 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | Proficient Rx LP | 3522bdcc-8113-4562-8ca1-f3eb884beaea | 2026-06-01 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | Major Pharmaceuticals | a65b5fb3-ca3c-4226-9caa-42fb9a2f7373 | 2026-05-28 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | PD-Rx Pharmaceuticals, Inc. | ace2bb56-4992-49fe-9311-535b12eea9b4 | 2026-05-27 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | PD-Rx Pharmaceuticals, Inc. | 78c4551c-b922-43c9-9a5a-66377ea07bc2 | 2026-05-27 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | Redpharm Drug | 52614168-3a9e-335d-e063-6394a90ac27f | 2026-05-22 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Camber Pharmaceuticals, Inc. | dc1c1ddb-f16b-4d7a-aabe-cf8bdf8b7998 | 2026-05-22 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Torrent Pharmaceuticals Limited | 1bc081f2-399d-43fa-9e0f-9f8df0118e99 | 2026-05-21 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | A-S Medication Solutions | 9143e0ab-0fa1-4718-919c-ddfd1e9b8386 | 2026-05-21 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Camber Pharmaceuticals, Inc. | 96ab1605-e171-4e86-b357-2d9378f7a05a | 2026-05-18 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | NuCare Pharmaceuticals, Inc. | 36da8e3a-d17c-e42f-e063-6394a90a1ece | 2026-05-18 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | A-S Medication Solutions | a10b7ec1-bb59-4906-b32d-fbd2a17ed7a8 | 2026-05-17 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | A-S Medication Solutions | 18bd4315-2446-415b-a6a3-991ba0035768 | 2026-05-17 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | Umedica Laboratories USA Inc. | 90477a51-63ba-43f4-a74b-4659a946093c | 2026-05-13 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Golden State Medical Supply, Inc. | 512d1dbe-2d07-b3e0-e063-6394a90ae008 | 2026-05-06 | Warnings, Adverse reactions | BW9B0ZE037 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.