NDC 47335-062 – Dofetilide
Dofetilide .25 mg/1 · Capsule · Oral
Product NDC47335-062
Product details
- Brand name
- Dofetilide
- Generic name
- Dofetilide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA210466
- Marketed since
- October 11, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Dofetilide .25 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 47335-062-79 | 4 BLISTER PACK in 1 CARTON (47335-062-79) / 10 CAPSULE in 1 BLISTER PACK (47335-062-66) | Oct 11, 2018 |
| 47335-062-86 | 60 CAPSULE in 1 BOTTLE (47335-062-86) | Oct 11, 2018 |
Recalls mentioning this NDC
- D-1082-2023 Aug 16, 2023 · Class III
Out of Specification result observed in content uniformity testing
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