NDC 0135-0501-24
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
- 0135-0501
- Requested NDC
- 0135-0501-24
- Package NDCs from labels
- 0135-0501-24
- 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 |
|---|---|---|---|---|---|
| 0135-0501-06 | EA - Each | 0135-0501 | b09d8448-1a4c-4689-a621-6d971a52e230 | 1 | 2012-07-24 |
| 0135-0501-24 | EA - Each | 0135-0501 | 37c206fc-25d3-4017-8cfc-fd346d13bcee | 1 | 2012-07-24 |
| 0135-0501-50 | EA - Each | 0135-0501 | 3661b72c-f1b6-453d-875b-8392633a5402 | 1 | 2012-07-24 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.