NDC 55289-228-01
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
- 55289-228
- Requested NDC
- 55289-228-01
- Package NDCs from labels
- 55289-228-01
- Manufacturer
- National Council for Prescription Drug Programs
- Effective date
- 2012-07-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55289-228-01 | EA - Each | 55289-228 | f33d6cb0-cba9-4bff-a1d4-dcf4b167fcf0 | 1 | 2012-07-24 |
| 55289-228-03 | EA - Each | 55289-228 | e0e42f45-8237-4a2e-b321-b072dd549d78 | 1 | 2012-07-24 |
| 55289-228-06 | EA - Each | 55289-228 | 46b5cac7-036c-4d61-acfb-2241dfb2c744 | 1 | 2012-07-24 |
| 55289-228-14 | EA - Each | 55289-228 | 5b431b2a-c171-4913-a8ed-72bfd6f8e5d9 | 1 | 2012-07-24 |
| 55289-228-30 | EA - Each | 55289-228 | f011c92a-08cb-48f0-b730-202e9d9412f2 | 1 | 2012-07-24 |
| 55289-228-60 | EA - Each | 55289-228 | ebc5e5fb-78f6-4a32-ba5c-cd491424a25c | 1 | 2012-07-24 |
| 55289-228-90 | EA - Each | 55289-228 | f6475edf-e74d-4c01-b1ee-84a6077d6171 | 1 | 2012-07-24 |
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 |
|---|---|---|---|---|---|---|
| Atenolol | ATENOLOL | Ipca Laboratories Limited | 98d29958-b026-4888-a516-7bb85bb7d479 | 2026-01-21 | Boxed warning, Warnings, Adverse reactions | ANDA077877 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.