| 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 |