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HESPAN
HESPAN - 0264-1965-10 - (Hetastarch in Sodium Chloride)
Drug Information of HESPAN
| Product NDC: | 0264-1965 |
| Proprietary Name: | HESPAN |
| Non Proprietary Name: | Hetastarch in Sodium Chloride |
| Active Ingredient(s): | 6; .9 g/100mL; g/100mL & nbsp; Hetastarch in Sodium Chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HESPAN
| Product NDC: | 0264-1965 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA890105 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19910404 |
Package Information of HESPAN
| Package NDC: | 0264-1965-10 |
| Package Description: | 12 CONTAINER in 1 CASE (0264-1965-10) > 500 mL in 1 CONTAINER |
NDC Information of HESPAN
| NDC Code | 0264-1965-10 |
| Proprietary Name | HESPAN |
| Package Description | 12 CONTAINER in 1 CASE (0264-1965-10) > 500 mL in 1 CONTAINER |
| Product NDC | 0264-1965 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hetastarch in Sodium Chloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19910404 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | HETASTARCH; SODIUM CHLORIDE |
| Strength Number | 6; .9 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes | Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [Chemical/Ingredient] |
