FDA Application
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NDC Search Results on Active Ingredient: Amiodarone
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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AMIODARONE HYDROCHLORIDE | 43066-360-20 | Baxter Healthcare Corporation | NDA022325 | HUMAN PRESCRIPTION DRUG | NDA |
AMIODARONE HYDROCHLORIDE | 43066-150-10 | Baxter Healthcare Corporation | NDA022325 | HUMAN PRESCRIPTION DRUG | NDA |
AMIODARONE HYDROCHLORIDE | 72162-2148-3 | Bryant Ranch Prepack | ANDA075135 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-1985-2 | Bryant Ranch Prepack | ANDA078578 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 63629-2001-1 | Bryant Ranch Prepack | ANDA077069 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-1985-3 | Bryant Ranch Prepack | ANDA078578 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 63629-2076-1 | Bryant Ranch Prepack | ANDA077069 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-1985-4 | Bryant Ranch Prepack | ANDA078578 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-0881-5 | Bryant Ranch Prepack | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-0881-3 | Bryant Ranch Prepack | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-1985-1 | Bryant Ranch Prepack | ANDA078578 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-0881-4 | Bryant Ranch Prepack | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-0881-2 | Bryant Ranch Prepack | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-1985-5 | Bryant Ranch Prepack | ANDA078578 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-0881-1 | Bryant Ranch Prepack | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 52533-101-58 | Cantrell Drug Company | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
AMIODARONE HYDROCHLORIDE | 52533-101-59 | Cantrell Drug Company | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
AMIODARONE HYDROCHLORIDE | 55154-3365-0 | Cardinal Health 107, LLC | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 55154-8185-0 | Cardinal Health 107, LLC | ANDA204742 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 62135-578-30 | Chartwell RX, LLC | ANDA077069 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 62135-577-60 | Chartwell RX, LLC | ANDA077069 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 62135-576-30 | Chartwell RX, LLC | ANDA077069 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 70934-280-30 | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | ANDA204742 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 75907-006-60 | Dr. Reddy's Labratories Inc. | ANDA075389 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 75907-007-30 | Dr. Reddy's Labratories Inc. | ANDA075389 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 75907-006-05 | Dr. Reddy's Labratories Inc. | ANDA075389 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 75907-005-30 | Dr. Reddy's Labratories Inc. | ANDA075389 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 63323-616-09 | Fresenius Kabi USA, LLC | ANDA075761 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 63323-616-02 | Fresenius Kabi USA, LLC | ANDA075761 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 63323-616-03 | Fresenius Kabi USA, LLC | ANDA075761 | HUMAN PRESCRIPTION DRUG | ANDA |
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