| Product NDC: | 0338-0013 |
| Proprietary Name: | Sterile Water |
| Non Proprietary Name: | Water |
| Active Ingredient(s): | 100 mL/100mL & nbsp; Water |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0338-0013 |
| Labeler Name: | BAXTER HEALTHCARE CORPORATION |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA018632 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19820630 |
| Package NDC: | 0338-0013-08 |
| Package Description: | 3000 mL in 1 BAG (0338-0013-08) |
| NDC Code | 0338-0013-08 |
| Proprietary Name | Sterile Water |
| Package Description | 3000 mL in 1 BAG (0338-0013-08) |
| Product NDC | 0338-0013 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Water |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19820630 |
| Marketing Category Name | ANDA |
| Labeler Name | BAXTER HEALTHCARE CORPORATION |
| Substance Name | WATER |
| Strength Number | 100 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |