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Sorbitol-Mannitol
Sorbitol-Mannitol - 0409-7981-08 - (Sorbitol and Mannitol)
Drug Information of Sorbitol-Mannitol
| Product NDC: | 0409-7981 |
| Proprietary Name: | Sorbitol-Mannitol |
| Non Proprietary Name: | Sorbitol and Mannitol |
| Active Ingredient(s): | .54; 2.7 g/100mL; g/100mL & nbsp; Sorbitol and Mannitol |
| Administration Route(s): | URETHRAL |
| Dosage Form(s): | IRRIGANT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sorbitol-Mannitol
| Product NDC: | 0409-7981 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA018316 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100408 |
Package Information of Sorbitol-Mannitol
| Package NDC: | 0409-7981-08 |
| Package Description: | 4 BAG in 1 CASE (0409-7981-08) > 3000 mL in 1 BAG |
NDC Information of Sorbitol-Mannitol
| NDC Code | 0409-7981-08 |
| Proprietary Name | Sorbitol-Mannitol |
| Package Description | 4 BAG in 1 CASE (0409-7981-08) > 3000 mL in 1 BAG |
| Product NDC | 0409-7981 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sorbitol and Mannitol |
| Dosage Form Name | IRRIGANT |
| Route Name | URETHRAL |
| Start Marketing Date | 20100408 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | MANNITOL; SORBITOL |
| Strength Number | .54; 2.7 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes | Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC] |
