NDC 51079-672-01
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
- 51079-672
- Requested NDC
- 51079-672-01
- Package NDCs from labels
- 51079-672-01
- 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 |
|---|---|---|---|---|---|
| 51079-672-01 | EA - Each | 51079-672 | 4cd5183f-71ed-4f54-927a-4bc1e06dd6d3 | 1 | 2012-07-24 |
| 51079-672-20 | EA - Each | 51079-672 | dccd5906-7e73-4b75-a2a3-803a9b76d473 | 1 | 2012-07-24 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.