NDC 70914-030-01 - Alzair
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
- 70914-030
- Requested NDC
- 70914-030-01
- Package NDCs from labels
- 70914-030-01
- Manufacturer
- Hudson Scientific LLC
- Effective date
- 2021-01-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Alzair - Hudson Scientific LLC | Hudson Scientific LLC | 2021-01-11 | MEDICAL DEVICE |
| Alzair - Hudson Scientific LLC | Hudson Scientific LLC | 2018-05-19 | MEDICAL DEVICE |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70914-030-01 | EA - Each | 70914-030 | e6a81cdc-6848-4795-9d20-e008b9535530 | 1 | 2018-04-19 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.