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Furosemide
Furosemide - 0409-1639-10 - (FUROSEMIDE)
Drug Information of Furosemide
| Product NDC: | 0409-1639 |
| Proprietary Name: | Furosemide |
| Non Proprietary Name: | FUROSEMIDE |
| Active Ingredient(s): | 10 mg/mL & nbsp; FUROSEMIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Furosemide
| Product NDC: | 0409-1639 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075241 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990528 |
Package Information of Furosemide
| Package NDC: | 0409-1639-10 |
| Package Description: | 10 CARTON in 1 CONTAINER (0409-1639-10) > 1 SYRINGE, PLASTIC in 1 CARTON > 10 mL in 1 SYRINGE, PLASTIC |
NDC Information of Furosemide
| NDC Code | 0409-1639-10 |
| Proprietary Name | Furosemide |
| Package Description | 10 CARTON in 1 CONTAINER (0409-1639-10) > 1 SYRINGE, PLASTIC in 1 CARTON > 10 mL in 1 SYRINGE, PLASTIC |
| Product NDC | 0409-1639 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FUROSEMIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19990528 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | FUROSEMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
