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Sodium Chloride
Sodium Chloride - 0409-6660-75 - (SODIUM CHLORIDE)
Drug Information of Sodium Chloride
| Product NDC: | 0409-6660 |
| Proprietary Name: | Sodium Chloride |
| Non Proprietary Name: | SODIUM CHLORIDE |
| Active Ingredient(s): | 5.84 g/40mL & nbsp; SODIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chloride
| Product NDC: | 0409-6660 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018897 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100825 |
Package Information of Sodium Chloride
| Package NDC: | 0409-6660-75 |
| Package Description: | 25 VIAL in 1 TRAY (0409-6660-75) > 40 mL in 1 VIAL |
NDC Information of Sodium Chloride
| NDC Code | 0409-6660-75 |
| Proprietary Name | Sodium Chloride |
| Package Description | 25 VIAL in 1 TRAY (0409-6660-75) > 40 mL in 1 VIAL |
| Product NDC | 0409-6660 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100825 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 5.84 |
| Strength Unit | g/40mL |
| Pharmaceutical Classes |
