Product NDC: | 52584-702 |
Proprietary Name: | Furosemide |
Non Proprietary Name: | Furosemide |
Active Ingredient(s): | 10 mg/mL & nbsp; Furosemide |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-702 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018579 |
Marketing Category: | NDA |
Start Marketing Date: | 20100801 |
Package NDC: | 52584-702-25 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-702-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 52584-702-25 |
Proprietary Name | Furosemide |
Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-702-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 52584-702 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Furosemide |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20100801 |
Marketing Category Name | NDA |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | FUROSEMIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |