Home
>
National Drug Code (NDC)
>
Sodium Chloride
Sodium Chloride - 0338-6304-04 - (Sodium Chloride)
Drug Information of Sodium Chloride
| Product NDC: | 0338-6304 |
| Proprietary Name: | Sodium Chloride |
| Non Proprietary Name: | Sodium Chloride |
| Active Ingredient(s): | 900 mg/100mL & nbsp; Sodium Chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chloride
| Product NDC: | 0338-6304 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016677 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19701209 |
Package Information of Sodium Chloride
| Package NDC: | 0338-6304-04 |
| Package Description: | 1000 mL in 1 BAG (0338-6304-04) |
NDC Information of Sodium Chloride
| NDC Code | 0338-6304-04 |
| Proprietary Name | Sodium Chloride |
| Package Description | 1000 mL in 1 BAG (0338-6304-04) |
| Product NDC | 0338-6304 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Chloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19701209 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 900 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
