Amiodarone Hydrochloride (Amiodarone Hydrochloride) — NDC 51672-4025 by Sun Pharmaceutical Industries, Inc.
Amiodarone Hydrochloride (Amiodarone Hydrochloride) — NDC 51672-4025 by Sun Pharmaceutical Industries, Inc. is one of 9,000 drug products in the NDCLookup dataset. Key details — Brand name: Amiodarone Hydrochloride; Generic name: Amiodarone Hydrochloride; Product NDC: 51672-4025.
| Brand name | Amiodarone Hydrochloride |
|---|---|
| Generic name | Amiodarone Hydrochloride |
| Product NDC | 51672-4025 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Dosage form | TABLET |
| Route | ORAL |
| Active ingredients | AMIODARONE HYDROCHLORIDE 200 mg/1 |
| Pharmacologic class | Antiarrhythmic [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], P-Glycoprotein Inhibitors [ |
| Marketing category | ANDA |
| Product type | HUMAN PRESCRIPTION DRUG |
| Source | openFDA NDC Directory |
$899/mo
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