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Eplerenone
Eplerenone - 0185-5368-30 - (Eplerenone)
Drug Information of Eplerenone
| Product NDC: | 0185-5368 |
| Proprietary Name: | Eplerenone |
| Non Proprietary Name: | Eplerenone |
| Active Ingredient(s): | 25 mg/1 & nbsp; Eplerenone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Eplerenone
| Product NDC: | 0185-5368 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078510 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080801 |
Package Information of Eplerenone
| Package NDC: | 0185-5368-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (0185-5368-30) |
NDC Information of Eplerenone
| NDC Code | 0185-5368-30 |
| Proprietary Name | Eplerenone |
| Package Description | 30 TABLET in 1 BOTTLE (0185-5368-30) |
| Product NDC | 0185-5368 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Eplerenone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080801 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | EPLERENONE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA] |
