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DILUENT
DILUENT - 0173-0518-01 - (water)
Drug Information of DILUENT
| Product NDC: | 0173-0518 |
| Proprietary Name: | DILUENT |
| Non Proprietary Name: | water |
| Active Ingredient(s): | 1 mL/mL & nbsp; water |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DILUENT
| Product NDC: | 0173-0518 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020444 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030506 |
Package Information of DILUENT
| Package NDC: | 0173-0518-01 |
| Package Description: | 2 VIAL in 1 TRAY (0173-0518-01) > 50 mL in 1 VIAL |
NDC Information of DILUENT
| NDC Code | 0173-0518-01 |
| Proprietary Name | DILUENT |
| Package Description | 2 VIAL in 1 TRAY (0173-0518-01) > 50 mL in 1 VIAL |
| Product NDC | 0173-0518 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | water |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20030506 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | WATER |
| Strength Number | 1 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
