NDC 63402-675-02 - ARCAPTA NEOHALER
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
- 63402-675
- Requested NDC
- 63402-675-02
- Package NDCs from labels
- 63402-675-01, 63402-675-30, 63402-675-02, 63402-675-06
- Manufacturer
- Sunovion Pharmaceuticals Inc.
- Effective date
- 2020-05-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ARCAPTA NEOHALER - Sunovion Pharmaceuticals Inc. | Sunovion Pharmaceuticals Inc. | 2020-05-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63402-675-01 | EA - Each | 63402-675 | 2c1ee963-4476-4518-a6b1-aa4a6d876e43 | 1 | 2018-01-12 |
| 63402-675-30 | EA - Each | 63402-675 | ad3b7f59-f8f5-4beb-b06f-9e7bccdc168d | 1 | 2018-01-12 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| b68719dc-6a70-44d8-bee7-7b96ca58a8ad | e82416ba-23b9-4d40-a41d-baba8e11751b | 2021-07-30 | Warnings, Adverse reactions | e82416ba-23b9-4d40-a41d-baba8e11751b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.