Flecainide Acetate
- Product NDC
- 50090-1132
- 11-digit product format
- 500901132
- Labeler code
- 50090
- Product ID
- 50090-1132_bbb125e9-9460-474c-b398-598c0ba58c45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- flecainide acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076278
- Marketing category
- ANDA
- Marketing start
- 2003-01-14
- Marketing end
- 0000-00-00
- Substance
- FLECAINIDE ACETATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1132-0 | 50090113200 | 60 TABLET in 1 BOTTLE (50090-1132-0) | 60 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |