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Hetastarch in Sodium Chloride
Hetastarch in Sodium Chloride - 0409-7248-49 - (HETASTARCH)
Drug Information of Hetastarch in Sodium Chloride
| Product NDC: | 0409-7248 |
| Proprietary Name: | Hetastarch in Sodium Chloride |
| Non Proprietary Name: | HETASTARCH |
| Active Ingredient(s): | 6 g/100mL & nbsp; HETASTARCH |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hetastarch in Sodium Chloride
| Product NDC: | 0409-7248 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA740193 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050228 |
Package Information of Hetastarch in Sodium Chloride
| Package NDC: | 0409-7248-49 |
| Package Description: | 12 BAG in 1 CASE (0409-7248-49) > 500 mL in 1 BAG |
NDC Information of Hetastarch in Sodium Chloride
| NDC Code | 0409-7248-49 |
| Proprietary Name | Hetastarch in Sodium Chloride |
| Package Description | 12 BAG in 1 CASE (0409-7248-49) > 500 mL in 1 BAG |
| Product NDC | 0409-7248 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HETASTARCH |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050228 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | HETASTARCH |
| Strength Number | 6 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes | Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [Chemical/Ingredient] |
