NDC 51672-4055 – Amiodarone Hydrochloride
Amiodarone Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC51672-4055
Product details
- Brand name
- Amiodarone Hydrochloride
- Generic name
- Amiodarone Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075424
- Marketed since
- March 30, 2001
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Amiodarone Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Amiodarone Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4055-6 | 30 TABLET in 1 BOTTLE (51672-4055-6) | Mar 30, 2001 |
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