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Furosemide
Furosemide - 63739-464-05 - (furosemide)
Drug Information of Furosemide
| Product NDC: | 63739-464 |
| Proprietary Name: | Furosemide |
| Non Proprietary Name: | furosemide |
| Active Ingredient(s): | 20 mg/2mL & nbsp; furosemide |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Furosemide
| Product NDC: | 63739-464 |
| Labeler Name: | McKesson Packaging Services Business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018579 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100201 |
Package Information of Furosemide
| Package NDC: | 63739-464-05 |
| Package Description: | 5 BAG in 1 BOX (63739-464-05) > 1 VIAL, SINGLE-DOSE in 1 BAG > 4 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Furosemide
| NDC Code | 63739-464-05 |
| Proprietary Name | Furosemide |
| Package Description | 5 BAG in 1 BOX (63739-464-05) > 1 VIAL, SINGLE-DOSE in 1 BAG > 4 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63739-464 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | furosemide |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20100201 |
| Marketing Category Name | NDA |
| Labeler Name | McKesson Packaging Services Business unit of McKesson Corporation |
| Substance Name | FUROSEMIDE |
| Strength Number | 20 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
