Product NDC: | 0054-3294 |
Proprietary Name: | Furosemide |
Non Proprietary Name: | Furosemide |
Active Ingredient(s): | 10 mg/mL & nbsp; Furosemide |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-3294 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070434 |
Marketing Category: | ANDA |
Start Marketing Date: | 19880712 |
Package NDC: | 0054-3294-46 |
Package Description: | 60 mL in 1 BOTTLE, DROPPER (0054-3294-46) |
NDC Code | 0054-3294-46 |
Proprietary Name | Furosemide |
Package Description | 60 mL in 1 BOTTLE, DROPPER (0054-3294-46) |
Product NDC | 0054-3294 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Furosemide |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19880712 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | FUROSEMIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |