Product NDC: | 0703-9258 |
Proprietary Name: | Sterile Diluent |
Non Proprietary Name: | Sterile Diluent |
Active Ingredient(s): | 1 mL/mL & nbsp; Sterile Diluent |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0703-9258 |
Labeler Name: | Teva Parenteral Medicines, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078396 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080423 |
Package NDC: | 0703-9258-09 |
Package Description: | 2 VIAL in 1 TRAY (0703-9258-09) > 50 mL in 1 VIAL (0703-9258-01) |
NDC Code | 0703-9258-09 |
Proprietary Name | Sterile Diluent |
Package Description | 2 VIAL in 1 TRAY (0703-9258-09) > 50 mL in 1 VIAL (0703-9258-01) |
Product NDC | 0703-9258 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sterile Diluent |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20080423 |
Marketing Category Name | ANDA |
Labeler Name | Teva Parenteral Medicines, Inc. |
Substance Name | WATER |
Strength Number | 1 |
Strength Unit | mL/mL |
Pharmaceutical Classes |