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Inspra
Inspra - 21695-797-90 - (eplerenone)
Drug Information of Inspra
| Product NDC: | 21695-797 |
| Proprietary Name: | Inspra |
| 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 Inspra
| Product NDC: | 21695-797 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021437 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020927 |
Package Information of Inspra
| Package NDC: | 21695-797-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (21695-797-90) |
NDC Information of Inspra
| NDC Code | 21695-797-90 |
| Proprietary Name | Inspra |
| Package Description | 90 TABLET in 1 BOTTLE (21695-797-90) |
| Product NDC | 21695-797 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | eplerenone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020927 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | EPLERENONE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA] |
