| Product NDC: | 0264-4002 |
| Proprietary Name: | SODIUM CHLORIDE |
| Non Proprietary Name: | SODIUM CHLORIDE |
| Active Ingredient(s): | .9 g/100mL & nbsp; SODIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0264-4002 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110311 |
| Package NDC: | 0264-4002-55 |
| Package Description: | 12 CONTAINER in 1 CASE (0264-4002-55) > 150 mL in 1 CONTAINER |
| NDC Code | 0264-4002-55 |
| Proprietary Name | SODIUM CHLORIDE |
| Package Description | 12 CONTAINER in 1 CASE (0264-4002-55) > 150 mL in 1 CONTAINER |
| Product NDC | 0264-4002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM CHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110311 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | .9 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |