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Furosemide
Furosemide - 0781-1966-01 - (Furosemide)
Drug Information of Furosemide
| 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) |
Labeler Information of Furosemide
| 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 Information of Furosemide
| Package NDC: | 0781-1966-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0781-1966-01) |
NDC Information of Furosemide
| NDC Code | 0781-1966-01 |
| Proprietary Name | Furosemide |
| Package Description | 100 TABLET in 1 BOTTLE (0781-1966-01) |
| 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] |
