Prescription drug · ANDA
Dofetilide 0.5mg NDC 70010-026
Dofetilide .5 mg/1 · Capsule · Oral · Granules Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70010-026-06 | 70010002606 | 60 CAPSULE in 1 BOTTLE (70010-026-06)Marketed from Nov 14, 2024 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Dofetilide 0.5mg
- Generic name (nonproprietary)
- dofetilide 0.5mg
- Active ingredients
- Dofetilide — .5 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 212750
- Marketing start
- Listing expires
- Identifiers
- Product ID 70010-026_44f3f63d-4521-91e4-e063-6394a90a6d1bSPL ID 44f3f63d-4521-91e4-e063-6394a90a6d1bSPL set ID a10633a6-4518-4a87-a880-faaa33bdbec6RxCUI 310003, 310004, 310005UNII R4Z9X1N2NDUPC 0370010025066, 0370010026063
- Pharmacologic class
- Antiarrhythmic
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470010002606followed by a unit qualifier and the quantityPackage 70010-0026-06. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Maintenance of Normal Sinus Rhythm (Delay in AF/AFl Recurrence) Dofetilide capsule is indicated for the maintenance of normal sinus rhythm (delay in time to recurrence of atrial fibrillation/atrial flutter [AF/AFl]) in patients with atrial fibrillation/atrial flutter of greater than one week duration who have been converted to normal sinus rhythm. Because dofetilide capsule can cause life threatening ventricular arrhythmias, it should be reserved for patients in whom atrial fibrillation/atrial flutter is highly symptomatic. In general, antiarrhythmic therapy for atrial fibrillation/atrial flutter aims to prolong the time in normal sinus rhythm. Recurrence is expected in…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 212750
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Dofetilide 0.125mg | Dofetilide .125 mg/1 | CapsuleOral | Granules Pharmaceuticals Inc. | 70010-024 |
| Dofetilide 0.25mg | Dofetilide .25 mg/1 | CapsuleOral | Granules Pharmaceuticals Inc. | 70010-025 |
| Dofetilide | Dofetilide .125 mg/1 | CapsuleOral | EXELAN PHARMACEUTICALS, INC. | 76282-755 |
| Dofetilide | Dofetilide .25 mg/1 | CapsuleOral | EXELAN PHARMACEUTICALS, INC. | 76282-756 |
| Dofetilide | Dofetilide .5 mg/1 | CapsuleOral | EXELAN PHARMACEUTICALS, INC. | 76282-757 |