Product NDC: | 0781-1966 |
Proprietary Name: | Furosemide |
Non Proprietary Name: | Furosemide |
Active Ingredient(s): | 40 mg/1 & nbsp; Furosemide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-1966 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018569 |
Marketing Category: | NDA |
Start Marketing Date: | 19811019 |
Package NDC: | 0781-1966-60 |
Package Description: | 60 TABLET in 1 BOTTLE (0781-1966-60) |
NDC Code | 0781-1966-60 |
Proprietary Name | Furosemide |
Package Description | 60 TABLET in 1 BOTTLE (0781-1966-60) |
Product NDC | 0781-1966 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Furosemide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19811019 |
Marketing Category Name | NDA |
Labeler Name | Sandoz Inc |
Substance Name | FUROSEMIDE |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |