NDC 51672-4057 – Amiodarone Hydrochloride
Amiodarone Hydrochloride 400 mg/1 · Tablet · Oral
Product NDC51672-4057
Product details
- Brand name
- Amiodarone Hydrochloride
- Generic name
- Amiodarone Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076362
- Marketed since
- November 29, 2002
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Amiodarone Hydrochloride 400 mg/1
Uses, dosage, side effects and warnings for Amiodarone Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4057-0 | 10 BLISTER PACK in 1 CARTON (51672-4057-0) / 10 TABLET in 1 BLISTER PACK | Nov 29, 2002 |
| 51672-4057-6 | 30 TABLET in 1 BOTTLE (51672-4057-6) | Nov 29, 2002 |
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