Product NDC: | 0264-7805 |
Proprietary Name: | Sodium Chloride |
Non Proprietary Name: | Sodium Chloride |
Active Ingredient(s): | 3 g/100mL & nbsp; Sodium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0264-7805 |
Labeler Name: | B. Braun Medical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA019635 |
Marketing Category: | ANDA |
Start Marketing Date: | 19880319 |
Package NDC: | 0264-7805-10 |
Package Description: | 24 CONTAINER in 1 CASE (0264-7805-10) > 500 mL in 1 CONTAINER |
NDC Code | 0264-7805-10 |
Proprietary Name | Sodium Chloride |
Package Description | 24 CONTAINER in 1 CASE (0264-7805-10) > 500 mL in 1 CONTAINER |
Product NDC | 0264-7805 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Chloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19880319 |
Marketing Category Name | ANDA |
Labeler Name | B. Braun Medical Inc. |
Substance Name | SODIUM CHLORIDE |
Strength Number | 3 |
Strength Unit | g/100mL |
Pharmaceutical Classes |