Dofetilide
- Product NDC
- 71410-302
- 11-digit product format
- 714100302
- Labeler code
- 71410
- Product ID
- 71410-302_0a6273e5-224d-4205-a497-f67f8bdfe83a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dofetilide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Liberty Bioscience LLC
- Application
- ANDA207058
- Marketing category
- ANDA
- Marketing start
- 2016-06-07
- Marketing end
- 0000-00-00
- Substance
- DOFETILIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71410-302-06 | Dofetilide | 60 in 1 BOTTLE | CAPSULE | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71410-302 | DOFETILIDE CAPSULE [LIBERTY BIOSCIENCE LLC] | 5 | Legacy NDC, 1 package rows | 20190509_66c20086-5030-441e-842d-2eee0d1a2a3a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 71410-302-06 | 71410030206 | 60 in 1 BOTTLE | Historical |