NDC 65841-631 – Amiodarone hydrochloride
Amiodarone Hydrochloride 200 mg/1 · Tablet · Oral
Product NDC65841-631
Product details
- Brand name
- Amiodarone hydrochloride
- Generic name
- Amiodarone hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA079029
- Marketed since
- August 10, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Amiodarone Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Amiodarone Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65841-631-05 | 500 TABLET in 1 BOTTLE (65841-631-05) | Aug 10, 2009 |
| 65841-631-06 | 30 TABLET in 1 BOTTLE (65841-631-06) | Aug 10, 2009 |
| 65841-631-10 | 1000 TABLET in 1 BOTTLE (65841-631-10) | Aug 10, 2009 |
| 65841-631-14 | 60 TABLET in 1 BOTTLE (65841-631-14) | Aug 10, 2009 |
| 65841-631-77 | 10 BLISTER PACK in 1 CARTON (65841-631-77) / 10 TABLET in 1 BLISTER PACK | Aug 10, 2009 |
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