Home
>
National Drug Code (NDC)
>
Furosemide
Furosemide - 63323-280-04 - (FUROSEMIDE)
Drug Information of Furosemide
| Product NDC: | 63323-280 |
| 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: | 63323-280 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018902 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000712 |
Package Information of Furosemide
| Package NDC: | 63323-280-04 |
| Package Description: | 25 VIAL in 1 TRAY (63323-280-04) > 4 mL in 1 VIAL |
NDC Information of Furosemide
| NDC Code | 63323-280-04 |
| Proprietary Name | Furosemide |
| Package Description | 25 VIAL in 1 TRAY (63323-280-04) > 4 mL in 1 VIAL |
| Product NDC | 63323-280 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FUROSEMIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20000712 |
| Marketing Category Name | NDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | FUROSEMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
