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furosemide
furosemide - 21695-721-25 - (furosemide)
Drug Information of furosemide
| Product NDC: | 21695-721 |
| Proprietary Name: | furosemide |
| Non Proprietary Name: | furosemide |
| Active Ingredient(s): | 10 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: | 21695-721 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA018579 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19831130 |
Package Information of furosemide
| Package NDC: | 21695-721-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 BOX (21695-721-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of furosemide
| NDC Code | 21695-721-25 |
| Proprietary Name | furosemide |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 BOX (21695-721-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 21695-721 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | furosemide |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19831130 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | FUROSEMIDE |
| Strength Number | 10 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
