| 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: | 0338-0013-06 | 
| Package Description: | 2000 mL in 1 BAG (0338-0013-06) | 
| NDC Code | 0338-0013-06 | 
| Proprietary Name | Sterile Water | 
| Package Description | 2000 mL in 1 BAG (0338-0013-06) | 
| 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 |