NDC 68462-408 – Propafenone hydrochloride
Propafenone Hydrochloride 225 mg/1 · Capsule, Extended Release · Oral
Product NDC68462-408
Product details
- Brand name
- Propafenone hydrochloride
- Generic name
- Propafenone hydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205268
- Marketed since
- September 8, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Propafenone Hydrochloride 225 mg/1
Uses, dosage, side effects and warnings for Propafenone hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68462-408-60 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-408-60) | Sep 8, 2017 |
Recalls mentioning this NDC
- D-0316-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-0315-2025 Apr 16, 2025 · Class II
CGMP Deviations
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