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Sodium Chloride
Sodium Chloride - 63323-186-02 - (SODIUM CHLORIDE)
Drug Information of Sodium Chloride
| Product NDC: | 63323-186 |
| Proprietary Name: | Sodium Chloride |
| Non Proprietary Name: | SODIUM CHLORIDE |
| Active Ingredient(s): | 9 mg/mL & nbsp; SODIUM CHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chloride
| Product NDC: | 63323-186 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000810 |
Package Information of Sodium Chloride
| Package NDC: | 63323-186-02 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-186-02) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Sodium Chloride
| NDC Code | 63323-186-02 |
| Proprietary Name | Sodium Chloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-186-02) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-186 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM CHLORIDE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20000810 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 9 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
