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Cordarone
Cordarone - 0008-4188-04 - (AMIODARONE HYDROCHLORIDE)
Drug Information of Cordarone
| Product NDC: | 0008-4188 |
| Proprietary Name: | Cordarone |
| Non Proprietary Name: | AMIODARONE HYDROCHLORIDE |
| Active Ingredient(s): | 200 mg/1 & nbsp; AMIODARONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cordarone
| Product NDC: | 0008-4188 |
| Labeler Name: | Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018972 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19851201 |
Package Information of Cordarone
| Package NDC: | 0008-4188-04 |
| Package Description: | 60 TABLET in 1 BOTTLE (0008-4188-04) |
NDC Information of Cordarone
| NDC Code | 0008-4188-04 |
| Proprietary Name | Cordarone |
| Package Description | 60 TABLET in 1 BOTTLE (0008-4188-04) |
| Product NDC | 0008-4188 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMIODARONE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19851201 |
| Marketing Category Name | NDA |
| Labeler Name | Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc. |
| Substance Name | AMIODARONE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
