Product NDC: | 0409-4090 |
Proprietary Name: | ZINC |
Non Proprietary Name: | ZINC CHLORIDE |
Active Ingredient(s): | 1 mg/mL & nbsp; ZINC CHLORIDE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-4090 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018959 |
Marketing Category: | NDA |
Start Marketing Date: | 20110811 |
Package NDC: | 0409-4090-01 |
Package Description: | 1 TRAY in 1 CASE (0409-4090-01) > 25 VIAL, PLASTIC in 1 TRAY > 10 mL in 1 VIAL, PLASTIC |
NDC Code | 0409-4090-01 |
Proprietary Name | ZINC |
Package Description | 1 TRAY in 1 CASE (0409-4090-01) > 25 VIAL, PLASTIC in 1 TRAY > 10 mL in 1 VIAL, PLASTIC |
Product NDC | 0409-4090 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ZINC CHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110811 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | ZINC CHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes |