Amiodarone hydrochloride
- Product NDC
- 55154-7890
- 11-digit product format
- 551547890
- Labeler code
- 55154
- Product ID
- 55154-7890_783ca12f-8972-4f27-af9e-671e7c03fe35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amiodarone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA079029
- Marketing category
- ANDA
- Marketing start
- 2009-08-10
- Marketing end
- 2020-10-31
- Substance
- AMIODARONE HYDROCHLORIDE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Antiarrhythmic [EPC],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 1A2 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record