NDC 16571-736 – Propafenone Hydrochloride
Propafenone Hydrochloride 225 mg/1 · Capsule, Extended Release · Oral
Product NDC16571-736
Product details
- Brand name
- Propafenone Hydrochloride
- Generic name
- Propafenone Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205956
- Marketed since
- December 16, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Propafenone Hydrochloride 225 mg/1
Uses, dosage, side effects and warnings for Propafenone hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16571-736-06 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16571-736-06) | Dec 16, 2020 |
| 16571-736-50 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16571-736-50) | Dec 16, 2020 |
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