Flecainide Acetate
- Product NDC
- 68151-1464
- 11-digit product format
- 681511464
- Labeler code
- 68151
- Product ID
- 68151-1464_7f7c44bd-f26b-487b-bde1-3496c011b1ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- flecainide acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA076278
- Marketing category
- ANDA
- Marketing start
- 2003-01-14
- Marketing end
- 0000-00-00
- Substance
- FLECAINIDE ACETATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-1464-2 | Flecainide Acetate | 1 in 1 PACKAGE | TABLET | 1 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-1464 | FLECAINIDE ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20170706_399dc6c2-c7cf-4cdc-95cd-2eb1d7672663.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-1464-2 | 68151146402 | 1 in 1 PACKAGE | Historical |