Amiodarone Hydrochloride 71335-0881
Product NDC
71335-0881- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 30, 2001
- Listing Expires
- December 31, 2026
- Application
- ANDA075424
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amiodarone Hydrochloride | 200 mg/1 |
Drug Class
Antiarrhythmic [EPC]Cytochrome P450 1A2 Inhibitors [MoA]Cytochrome P450 2C9 Inhibitors [MoA]
Packaging Options(5)
200 TABLET in 1 BOTTLE (71335-0881-1)
30 TABLET in 1 BOTTLE (71335-0881-2)
60 TABLET in 1 BOTTLE (71335-0881-3)
90 TABLET in 1 BOTTLE (71335-0881-4)
10 TABLET in 1 BOTTLE (71335-0881-5)