HESPAN is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by B. Braun Medical Inc.. The primary component is Hetastarch; Sodium Chloride.
| Product ID | 0264-1965_47e5d437-857d-4328-bdda-e6ff01544d9d |
| NDC | 0264-1965 |
| Product Type | Human Prescription Drug |
| Proprietary Name | HESPAN |
| Generic Name | Hetastarch In Sodium Chloride |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 1991-04-04 |
| Marketing Category | NDA / NDA |
| Application Number | BN890105 |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | HETASTARCH; SODIUM CHLORIDE |
| Active Ingredient Strength | 6 g/100mL; g/100mL |
| Pharm Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 1991-04-04 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | BN890105 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1991-04-04 |
| Ingredient | Strength |
|---|---|
| HETASTARCH | 6 g/100mL |
| SPL SET ID: | 6f90664e-f2ec-47ea-bfec-7be2bf2dc28c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HESPAN 72378335 0933806 Live/Registered |
AMERICAN HOSPITAL SUPPLY CORPORATION 1970-12-10 |