Product NDC: | 0409-7965 |
Proprietary Name: | Normosol-M and Dextrose |
Non Proprietary Name: | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE |
Active Ingredient(s): | 5; 21; 128; 234 g/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp; DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-7965 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA017610 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110906 |
Package NDC: | 0409-7965-09 |
Package Description: | 12 POUCH in 1 CASE (0409-7965-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG |
NDC Code | 0409-7965-09 |
Proprietary Name | Normosol-M and Dextrose |
Package Description | 12 POUCH in 1 CASE (0409-7965-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG |
Product NDC | 0409-7965 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110906 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | DEXTROSE MONOHYDRATE; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE |
Strength Number | 5; 21; 128; 234 |
Strength Unit | g/100mL; mg/100mL; mg/100mL; mg/100mL |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |