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Dextrose And Sodium Chloride
Dextrose And Sodium Chloride - 0264-7616-20 - (DEXTROSE and SODIUM CHLORIDE)
Drug Information of Dextrose And Sodium Chloride
| Product NDC: | 0264-7616 |
| Proprietary Name: | Dextrose And Sodium Chloride |
| Non Proprietary Name: | DEXTROSE and SODIUM CHLORIDE |
| Active Ingredient(s): | 5; .2 g/100mL; g/100mL & nbsp; DEXTROSE and SODIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose And Sodium Chloride
| Product NDC: | 0264-7616 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019631 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19880224 |
Package Information of Dextrose And Sodium Chloride
| Package NDC: | 0264-7616-20 |
| Package Description: | 24 CONTAINER in 1 CASE (0264-7616-20) > 250 mL in 1 CONTAINER |
NDC Information of Dextrose And Sodium Chloride
| NDC Code | 0264-7616-20 |
| Proprietary Name | Dextrose And Sodium Chloride |
| Package Description | 24 CONTAINER in 1 CASE (0264-7616-20) > 250 mL in 1 CONTAINER |
| Product NDC | 0264-7616 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXTROSE and SODIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19880224 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | DEXTROSE; SODIUM CHLORIDE |
| Strength Number | 5; .2 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes |
