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Dextrose and Sodium Chloride
Dextrose and Sodium Chloride - 0409-7941-03 - (DEXTROSE MONOHYDRATE and SODIUM CHLORIDE)
Drug Information of Dextrose and Sodium Chloride
| Product NDC: | 0409-7941 |
| Proprietary Name: | Dextrose and Sodium Chloride |
| Non Proprietary Name: | DEXTROSE MONOHYDRATE and SODIUM CHLORIDE |
| Active Ingredient(s): | 5; .9 g/100mL; g/100mL & nbsp; DEXTROSE MONOHYDRATE and SODIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose and Sodium Chloride
| Product NDC: | 0409-7941 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA017585 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110216 |
Package Information of Dextrose and Sodium Chloride
| Package NDC: | 0409-7941-03 |
| Package Description: | 24 POUCH in 1 CASE (0409-7941-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
NDC Information of Dextrose and Sodium Chloride
| NDC Code | 0409-7941-03 |
| Proprietary Name | Dextrose and Sodium Chloride |
| Package Description | 24 POUCH in 1 CASE (0409-7941-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
| Product NDC | 0409-7941 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXTROSE MONOHYDRATE and SODIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110216 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DEXTROSE MONOHYDRATE; SODIUM CHLORIDE |
| Strength Number | 5; .9 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes |
