Product NDC: | 52584-052 |
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: | 52584-052 |
Labeler Name: | General Injectables & Vaccines, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075241 |
Marketing Category: | ANDA |
Start Marketing Date: | 20010301 |
Package NDC: | 52584-052-10 |
Package Description: | 1 SYRINGE in 1 BAG (52584-052-10) > 10 mL in 1 SYRINGE |
NDC Code | 52584-052-10 |
Proprietary Name | Furosemide |
Package Description | 1 SYRINGE in 1 BAG (52584-052-10) > 10 mL in 1 SYRINGE |
Product NDC | 52584-052 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Furosemide |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20010301 |
Marketing Category Name | ANDA |
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] |