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Mannitol
Mannitol - 0517-4050-25 - (mannitol)
Drug Information of Mannitol
| Product NDC: | 0517-4050 |
| Proprietary Name: | Mannitol |
| Non Proprietary Name: | mannitol |
| Active Ingredient(s): | 250 mg/mL & nbsp; mannitol |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mannitol
| Product NDC: | 0517-4050 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087409 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Mannitol
| Package NDC: | 0517-4050-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4050-25) > 50 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Mannitol
| NDC Code | 0517-4050-25 |
| Proprietary Name | Mannitol |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4050-25) > 50 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-4050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mannitol |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | MANNITOL |
| Strength Number | 250 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC] |
