NDC 0781-7067-61
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
- 0781-7067
- Requested NDC
- 0781-7067-61
- Package NDCs from labels
- 0781-7067-61
- 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 |
|---|---|---|---|---|---|
| 0781-7067-30 | ML - Milliliter | 0781-7067 | e5ddc451-f46f-4905-8e9f-1b7253b84e09 | 1 | 2012-07-24 |
| 0781-7067-61 | ML - Milliliter | 0781-7067 | dcaf9a72-7ad8-4cf4-83ef-a39a5d830f2d | 1 | 2012-07-24 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.