Flecainide Acetate
- Product NDC
- 50090-2233
- 11-digit product format
- 500902233
- Labeler code
- 50090
- Product ID
- 50090-2233_d64099b1-9879-4d9f-b325-f23d16d120dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flecainide Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202821
- Marketing category
- ANDA
- Marketing start
- 2017-11-03
- Marketing end
- 0000-00-00
- Substance
- FLECAINIDE ACETATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2233-0 | Flecainide Acetate | 60 in 1 BOTTLE | TABLET | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2233 | FLECAINIDE ACETATE TABLET [A-S MEDICATION SOLUTIONS] | 5 | Legacy NDC, 1 package rows | 20210227_552ce99a-1195-4f53-971a-ad5874bba9d5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2233-0 | 50090223300 | 60 TABLET in 1 BOTTLE (50090-2233-0) | 60 tablet | 2017-11-03 | 0000-00-00 | No | No | Current |