HESPAN (B. Braun Medical Inc.)


Welcome to the PulseAid listing for the HESPAN drug offered from B. Braun Medical Inc.. This Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [Chemical/Ingredient],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: B. Braun Medical Inc.
NON-PROPRIETARY NAME: Hetastarch in Sodium Chloride
SUBSTANCE NAME: HETASTARCH; SODIUM CHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [Chemical/Ingredient],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1991-04-04
END MARKETING DATE: 0000-00-00


HESPAN HUMAN PRESCRIPTION DRUG Details:

Item DescriptionHESPAN from B. Braun Medical Inc.
LABELER NAME: B. Braun Medical Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 6; .9(g/100mL; g/100mL)
START MARKETING DATE: 1991-04-04
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0264-1965_5181c451-ce09-45e1-bb89-7190866c65d4
PRODUCT NDC: 0264-1965
APPLICATION NUMBER: BN890105

Other HETASTARCH; SODIUM CHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
B. Braun Medical Inc.HESPAN