Product NDC: | 0409-6138 |
Proprietary Name: | Sodium Chloride |
Non Proprietary Name: | SODIUM CHLORIDE |
Active Ingredient(s): | 900 mg/100mL & nbsp; SODIUM CHLORIDE |
Administration Route(s): | IRRIGATION |
Dosage Form(s): | IRRIGANT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-6138 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017514 |
Marketing Category: | NDA |
Start Marketing Date: | 20100517 |
Package NDC: | 0409-6138-22 |
Package Description: | 24 BOTTLE, PLASTIC in 1 CASE (0409-6138-22) > 250 mL in 1 BOTTLE, PLASTIC |
NDC Code | 0409-6138-22 |
Proprietary Name | Sodium Chloride |
Package Description | 24 BOTTLE, PLASTIC in 1 CASE (0409-6138-22) > 250 mL in 1 BOTTLE, PLASTIC |
Product NDC | 0409-6138 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM CHLORIDE |
Dosage Form Name | IRRIGANT |
Route Name | IRRIGATION |
Start Marketing Date | 20100517 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | SODIUM CHLORIDE |
Strength Number | 900 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |