NDC 51079-520-30
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
- 51079-520
- Requested NDC
- 51079-520-30
- Package NDCs from labels
- 51079-520-30
- 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 |
|---|---|---|---|---|---|
| 51079-520-01 | EA - Each | 51079-520 | 128467ea-8fc7-4c0b-8ead-d5e3e214ba3d | 1 | 2012-07-24 |
| 51079-520-20 | EA - Each | 51079-520 | bde3b5aa-18b0-4e40-9c36-630ffac1b612 | 1 | 2012-07-24 |
| 51079-520-30 | EA - Each | 51079-520 | 3c21bdfa-2db1-453c-aacf-ec740ee854ff | 1 | 2012-07-24 |
| 51079-520-56 | EA - Each | 51079-520 | 0b0aab6f-0c7d-46d7-9bb6-2ded3946a73c | 1 | 2012-07-24 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.