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EDECRIN
EDECRIN - 25010-215-15 - (ethacrynic acid)
Drug Information of EDECRIN
| Product NDC: | 25010-215 |
| Proprietary Name: | EDECRIN |
| Non Proprietary Name: | ethacrynic acid |
| Active Ingredient(s): | 25 mg/1 & nbsp; ethacrynic acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EDECRIN
| Product NDC: | 25010-215 |
| Labeler Name: | Aton Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016092 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19670110 |
Package Information of EDECRIN
| Package NDC: | 25010-215-15 |
| Package Description: | 100 TABLET in 1 BOTTLE (25010-215-15) |
NDC Information of EDECRIN
| NDC Code | 25010-215-15 |
| Proprietary Name | EDECRIN |
| Package Description | 100 TABLET in 1 BOTTLE (25010-215-15) |
| Product NDC | 25010-215 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ethacrynic acid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19670110 |
| Marketing Category Name | NDA |
| Labeler Name | Aton Pharma, Inc. |
| Substance Name | ETHACRYNIC ACID |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
