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Lasix
Lasix - 0039-0066-50 - (furosemide)
Drug Information of Lasix
| Product NDC: | 0039-0066 |
| Proprietary Name: | Lasix |
| Non Proprietary Name: | furosemide |
| Active Ingredient(s): | 80 mg/1 & nbsp; furosemide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lasix
| Product NDC: | 0039-0066 |
| Labeler Name: | Sanofi-Aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016273 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19660701 |
Package Information of Lasix
| Package NDC: | 0039-0066-50 |
| Package Description: | 500 TABLET in 1 BOTTLE (0039-0066-50) |
NDC Information of Lasix
| NDC Code | 0039-0066-50 |
| Proprietary Name | Lasix |
| Package Description | 500 TABLET in 1 BOTTLE (0039-0066-50) |
| Product NDC | 0039-0066 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | furosemide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19660701 |
| Marketing Category Name | NDA |
| Labeler Name | Sanofi-Aventis U.S. LLC |
| Substance Name | FUROSEMIDE |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
