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Normosol-M and Dextrose
Normosol-M and Dextrose - 0409-7965-03 - (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE)
Drug Information of Normosol-M and Dextrose
| 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) |
Labeler Information of Normosol-M and Dextrose
| 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 Information of Normosol-M and Dextrose
| Package NDC: | 0409-7965-03 |
| Package Description: | 24 POUCH in 1 CASE (0409-7965-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
NDC Information of Normosol-M and Dextrose
| NDC Code | 0409-7965-03 |
| Proprietary Name | Normosol-M and Dextrose |
| Package Description | 24 POUCH in 1 CASE (0409-7965-03) > 1 BAG in 1 POUCH > 500 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] |
