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Sodium Chloride
Sodium Chloride - 49349-764-01 - (SODIUM CHLORIDE)
Drug Information of Sodium Chloride
| Product NDC: | 49349-764 |
| 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) |
Labeler Information of Sodium Chloride
| Product NDC: | 49349-764 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018800 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130610 |
Package Information of Sodium Chloride
| Package NDC: | 49349-764-01 |
| Package Description: | 30 mL in 1 VIAL (49349-764-01) |
NDC Information of Sodium Chloride
| NDC Code | 49349-764-01 |
| Proprietary Name | Sodium Chloride |
| Package Description | 30 mL in 1 VIAL (49349-764-01) |
| Product NDC | 49349-764 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM CHLORIDE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20130610 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 9 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
