Product NDC: | 68084-016 |
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: | 68084-016 |
Labeler Name: | American Health Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076796 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060622 |
Package NDC: | 68084-016-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (68084-016-01) > 10 TABLET in 1 BLISTER PACK (68084-016-11) |
NDC Code | 68084-016-01 |
Proprietary Name | Furosemide |
Package Description | 10 BLISTER PACK in 1 CARTON (68084-016-01) > 10 TABLET in 1 BLISTER PACK (68084-016-11) |
Product NDC | 68084-016 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | furosemide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20060622 |
Marketing Category Name | ANDA |
Labeler Name | American Health Packaging |
Substance Name | FUROSEMIDE |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |