Dofetilide
- Product NDC
- 75907-055
- 11-digit product format
- 759070055
- Labeler code
- 75907
- Product ID
- 75907-055_861cea42-b727-d539-2e5d-aa7de6629fd4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dofetilide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Dr. Reddy's Labratories Inc.
- Application
- ANDA207058
- Marketing category
- ANDA
- Marketing start
- 2024-05-28
- Substance
- DOFETILIDE
- Active strength
- .25 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dofetilide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOFETILIDE | .25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R4Z9X1N2ND |
| Rxcui | 310003, 310004, 310005 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75907-055-60 | Dofetilide | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75907-055 | DOFETILIDE CAPSULE [DR. REDDY'S LABRATORIES INC.] | 1 | Current NDC, 1 package rows | 20240528_28fe0cac-62fd-997d-8065-561aaf1541c4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 75907-055-60 | 75907005560 | 60 CAPSULE in 1 BOTTLE, PLASTIC (75907-055-60) | 60 capsule | 2024-05-28 | No | No | Current |