NDC 51079-090-01
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
- 51079-090
- Requested NDC
- 51079-090-01
- Package NDCs from labels
- 51079-090-01
- 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 |
|---|---|---|---|---|---|
| 51079-090-01 | EA - Each | 51079-090 | f48792d8-9195-4edf-ac1b-81e4094a7dc8 | 1 | 2012-07-24 |
| 51079-090-20 | EA - Each | 51079-090 | 2272a342-105b-4fa4-82c0-1937c0a0faf2 | 1 | 2012-07-24 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.