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Sodium Edecrin
Sodium Edecrin - 25010-210-27 - (ethacrynate sodium)
Drug Information of Sodium Edecrin
| Product NDC: | 25010-210 |
| Proprietary Name: | Sodium Edecrin |
| Non Proprietary Name: | ethacrynate sodium |
| Active Ingredient(s): | 50 mg/50mL & nbsp; ethacrynate sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Edecrin
| Product NDC: | 25010-210 |
| Labeler Name: | Aton Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016093 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19670110 |
Package Information of Sodium Edecrin
| Package NDC: | 25010-210-27 |
| Package Description: | 1 VIAL in 1 CARTON (25010-210-27) > 50 mL in 1 VIAL |
NDC Information of Sodium Edecrin
| NDC Code | 25010-210-27 |
| Proprietary Name | Sodium Edecrin |
| Package Description | 1 VIAL in 1 CARTON (25010-210-27) > 50 mL in 1 VIAL |
| Product NDC | 25010-210 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ethacrynate sodium |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19670110 |
| Marketing Category Name | NDA |
| Labeler Name | Aton Pharma, Inc. |
| Substance Name | ETHACRYNATE SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/50mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
