Product NDC: | 55154-3183 |
Proprietary Name: | Sodium Chloride |
Non Proprietary Name: | Sodium Chloride |
Active Ingredient(s): | 9 mg/mL & nbsp; Sodium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-3183 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018800 |
Marketing Category: | NDA |
Start Marketing Date: | 19821029 |
Package NDC: | 55154-3183-8 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 BAG (55154-3183-8) > 30 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 55154-3183-8 |
Proprietary Name | Sodium Chloride |
Package Description | 1 VIAL, MULTI-DOSE in 1 BAG (55154-3183-8) > 30 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 55154-3183 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Chloride |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19821029 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | SODIUM CHLORIDE |
Strength Number | 9 |
Strength Unit | mg/mL |
Pharmaceutical Classes |