Home
>
National Drug Code (NDC)
>
Furosemide
Furosemide - 0517-5702-25 - (Furosemide)
Drug Information of Furosemide
| Product NDC: | 0517-5702 |
| Proprietary Name: | Furosemide |
| Non Proprietary Name: | Furosemide |
| Active Ingredient(s): | 10 mg/mL & nbsp; Furosemide |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Furosemide
| Product NDC: | 0517-5702 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA018579 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Furosemide
| Package NDC: | 0517-5702-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5702-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Furosemide
| NDC Code | 0517-5702-25 |
| Proprietary Name | Furosemide |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5702-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-5702 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Furosemide |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | FUROSEMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
