Dofetilide
- Product NDC
- 69539-131
- 11-digit product format
- 695390131
- Labeler code
- 69539
- Product ID
- 69539-131_6c77ee89-1263-47a5-9782-2ef5a58d24ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dofetilide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- MSN LABORATORIES PRIVATE LIMITED
- Application
- ANDA213220
- Marketing category
- ANDA
- Marketing start
- 2020-01-29
- Marketing end
- 0000-00-00
- Substance
- DOFETILIDE
- Active strength
- 0 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69539-131 | DOFETILIDE CAPSULE [MSN LABORATORIES PRIVATE LIMITED] | 2 | Legacy NDC | 20200212_1caa7d09-4d6c-4ccb-a44f-6f93a55fefe2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69539-131-38 | 69539013138 | 4 BLISTER PACK in 1 CARTON (69539-131-38) > 10 CAPSULE in 1 BLISTER PACK (69539-131-11) | 4 blister pack | 2020-01-29 | 0000-00-00 | No | No | Current |
| 69539-131-60 | 69539013160 | 60 CAPSULE in 1 BOTTLE (69539-131-60) | 60 capsule | 2020-01-29 | 0000-00-00 | No | No | Current |