NDC 71335-2995-01 - Flecainide Acetate
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
- 71335-2995
- Requested NDC
- 71335-2995-01
- Package NDCs from labels
- 71335-2995-1, 71335-2995-2, 71335-2995-3, 71335-2995-4, 71335-2995-5, 71335-2995-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2026-02-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Flecainide Acetate - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-02-04 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-2995-1 | Flecainide Acetate | 30 in 1 BOTTLE | TABLET | 30 | 1 | |
| 71335-2995-2 | Flecainide Acetate | 60 in 1 BOTTLE | TABLET | 60 | 1 | |
| 71335-2995-3 | Flecainide Acetate | 90 in 1 BOTTLE | TABLET | 90 | 1 | |
| 71335-2995-4 | Flecainide Acetate | 10 in 1 BOTTLE | TABLET | 10 | 1 | |
| 71335-2995-5 | Flecainide Acetate | 180 in 1 BOTTLE | TABLET | 180 | 1 |
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 |
|---|---|---|---|---|---|---|
| Flecainide Acetate | FLECAINIDE ACETATE TABLET | Bryant Ranch Prepack | 5dc5b522-f16f-4b3b-b325-f4ace495f966 | 2023-11-06 | Boxed warning, Warnings, Adverse reactions | 886662 M8U465Q1WQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.