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 CITRATE | SILDENAFIL CITRATE | NIVAGEN PHARMACEUTICALS, INC. | 5ac95dd0-57e4-495c-bf8d-b2e5bbe33e20 | 2026-04-27 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | Preferred Pharmaceuticals Inc. | 5f9ff0bb-5634-437a-96eb-249b910c7e81 | 2026-04-22 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals, Inc. | 48c56418-0e45-083f-e063-6294a90a57b3 | 2026-04-16 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | Bryant Ranch Prepack | a05ab4e7-6f70-41c3-a3b7-9a2fd7a1d2d6 | 2026-03-30 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals, Inc. | 4df47282-7950-9430-e063-6394a90af579 | 2026-03-26 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL | NuCare Pharmaceuticals,Inc. | fbe75c2c-0aff-9ade-e053-6394a90a1ea4 | 2026-03-20 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Jubilant Cadista Pharmaceuticals Inc. | 7d13bf00-8daf-3087-a0b8-abb1fc572467 | 2026-03-19 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | NuCare Pharmaceuticals,Inc. | cc3656ac-3a38-a650-e053-2a95a90a912a | 2026-03-16 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | Bryant Ranch Prepack | edb0919d-cbf1-4968-b0eb-342aa811c2ce | 2026-03-09 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | HEC Pharm USA Inc. | 4c57d855-3b49-fe6e-e063-6294a90a5cd5 | 2026-03-06 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL CITRATE | Northstar Rx LLC | 8127ff38-2761-49ec-8ce7-7f971f521cfb | 2026-02-26 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | Appco Pharma LLC | df1cc749-caec-4bf0-aa4d-db9dcc5257c3 | 2026-02-11 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL | SILDENAFIL | A-S Medication Solutions | e5ad3ce5-29ee-4b55-a67a-0f28c23a3afa | 2026-02-11 | Warnings, Adverse reactions | BW9B0ZE037 |
| SILDENAFIL CITRATE | SILDENAFIL | Torrent Pharmaceuticals Limited | b48630b1-5208-4d00-b56f-21701f223758 | 2026-02-10 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Bostal LLC | 428bbcff-0faf-499c-81b2-6ac76c0687c0 | 2026-02-04 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Reyoung Corporation | dc998a9c-0770-111b-e053-2a95a90a88a4 | 2026-02-04 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil | SILDENAFIL | Aurobindo Pharma Limited | 17621e92-79a0-46aa-86c7-ea179e81928d | 2026-02-03 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL CITRATE | Zydus Lifesciences Limited | 2ef4d02f-76ee-4f67-9f4f-1cd554decb31 | 2026-02-02 | Warnings, Adverse reactions | BW9B0ZE037 |
| sildenafil CITRATE | SILDENAFIL CITRATE | Aurobindo Pharma Limited | b60b4fdc-9b78-45e6-8438-8a30f83ed976 | 2026-02-02 | Warnings, Adverse reactions | BW9B0ZE037 |
| Sildenafil Citrate | SILDENAFIL CITRATE | Zydus Pharmaceuticals (USA) Inc. | b2f04ce4-f19c-403d-8a83-74f123e5d30a | 2026-02-02 | Warnings, Adverse reactions | BW9B0ZE037 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.