Product NDC: | 57826-441 |
Proprietary Name: | HAEMONETICS 0.9 % Sodium Chloride |
Non Proprietary Name: | SODIUM CHLORIDE |
Active Ingredient(s): | 900 mg/100mL & nbsp; SODIUM CHLORIDE |
Administration Route(s): | EXTRACORPOREAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57826-441 |
Labeler Name: | Haemonetics Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076316 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130107 |
Package NDC: | 57826-441-06 |
Package Description: | 500 mL in 1 BAG (57826-441-06) |
NDC Code | 57826-441-06 |
Proprietary Name | HAEMONETICS 0.9 % Sodium Chloride |
Package Description | 500 mL in 1 BAG (57826-441-06) |
Product NDC | 57826-441 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM CHLORIDE |
Dosage Form Name | SOLUTION |
Route Name | EXTRACORPOREAL |
Start Marketing Date | 20130107 |
Marketing Category Name | ANDA |
Labeler Name | Haemonetics Corporation |
Substance Name | SODIUM CHLORIDE |
Strength Number | 900 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |