NDC 51079-217-01
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
- 51079-217
- Requested NDC
- 51079-217-01
- Package NDCs from labels
- 51079-217-01
- Manufacturer
- National Council for Prescription Drug Programs
- Effective date
- 2013-02-13
- 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 | 2013-02-13 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51079-217-01 | EA - Each | 51079-217 | fc32e5c9-7b71-4006-9ae9-338bdb1fcfe5 | 1 | 2013-02-13 |
| 51079-217-17 | EA - Each | 51079-217 | fc0cadbc-a1ea-4c89-9b12-4aaf2e5b7108 | 1 | 2013-06-04 |
| 51079-217-19 | EA - Each | 51079-217 | 0e215369-3d6d-4ee4-a5a5-05ebdf64d667 | 1 | 2013-06-04 |
| 51079-217-20 | EA - Each | 51079-217 | 56c1fcd9-1b80-460f-bf3c-0b86f2e0afc2 | 1 | 2013-02-13 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.