Product NDC: | 76237-162 |
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: | 76237-162 |
Labeler Name: | McKesson Contract Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA018413 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111011 |
Package NDC: | 76237-162-30 |
Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-162-30) > 5 TABLET in 1 BLISTER PACK |
NDC Code | 76237-162-30 |
Proprietary Name | Furosemide |
Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-162-30) > 5 TABLET in 1 BLISTER PACK |
Product NDC | 76237-162 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Furosemide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20111011 |
Marketing Category Name | ANDA |
Labeler Name | McKesson Contract Packaging |
Substance Name | FUROSEMIDE |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |