Product NDC: | 55154-5701 |
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) |
Product NDC: | 55154-5701 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA018579 |
Marketing Category: | ANDA |
Start Marketing Date: | 19900930 |
Package NDC: | 55154-5701-5 |
Package Description: | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-5701-5) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 55154-5701-5 |
Proprietary Name | Furosemide |
Package Description | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-5701-5) > 2 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 55154-5701 |
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 | Cardinal Health |
Substance Name | FUROSEMIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |