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SODIUM CHLORIDE
SODIUM CHLORIDE - 0019-1188-75 - (sodium chloride)
Drug Information of SODIUM CHLORIDE
| Product NDC: | 0019-1188 |
| Proprietary Name: | SODIUM CHLORIDE |
| Non Proprietary Name: | sodium chloride |
| Active Ingredient(s): | .9 mg/mL & nbsp; sodium chloride |
| Administration Route(s): | INTRAVASCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM CHLORIDE
| Product NDC: | 0019-1188 |
| Labeler Name: | Mallinckrodt Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021569 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120901 |
Package Information of SODIUM CHLORIDE
| Package NDC: | 0019-1188-75 |
| Package Description: | 10 BOX in 1 CARTON (0019-1188-75) > 1 SYRINGE, PLASTIC in 1 BOX > 50 mL in 1 SYRINGE, PLASTIC |
NDC Information of SODIUM CHLORIDE
| NDC Code | 0019-1188-75 |
| Proprietary Name | SODIUM CHLORIDE |
| Package Description | 10 BOX in 1 CARTON (0019-1188-75) > 1 SYRINGE, PLASTIC in 1 BOX > 50 mL in 1 SYRINGE, PLASTIC |
| Product NDC | 0019-1188 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sodium chloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVASCULAR |
| Start Marketing Date | 20120901 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt Inc. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | .9 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
