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: | 0338-0013-29 |
Package Description: | 5000 mL in 1 BAG (0338-0013-29) |
NDC Code | 0338-0013-29 |
Proprietary Name | Sterile Water |
Package Description | 5000 mL in 1 BAG (0338-0013-29) |
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 |