NDC 0069-0181-01
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
- 0069-0181
- Requested NDC
- 0069-0181-01
- Package NDCs from labels
- 0069-0181-01
- 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 |
|---|---|---|---|---|---|
| 0069-0181-01 | ML - Milliliter | 0069-0181 | 50eece99-3988-46ea-ae08-43a4a850e78f | 1 | 2013-02-13 |
| 0069-0181-02 | ML - Milliliter | 0069-0181 | 2b8181d1-2b30-4ddc-aabd-8095c45111e3 | 1 | 2013-02-13 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.