NDC 0409-7248

Hetastarch in Sodium Chloride

Hetastarch

Hetastarch in Sodium Chloride is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Hetastarch.

Product ID0409-7248_472468e6-3ee8-444d-98ba-3ebaab2303af
NDC0409-7248
Product TypeHuman Prescription Drug
Proprietary NameHetastarch in Sodium Chloride
Generic NameHetastarch
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2005-02-28
Marketing CategoryANDA / ANDA
Application NumberBA740193
Labeler NameHospira, Inc.
Substance NameHETASTARCH
Active Ingredient Strength6 g/100mL
Pharm ClassesPlasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [CS]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0409-7248-03

12 CONTAINER in 1 CASE (0409-7248-03) > 500 mL in 1 CONTAINER (0409-7248-13)
Marketing Start Date2005-02-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0409-7248-03 [00409724803]

Hetastarch in Sodium Chloride INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberBA740193
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-02-28

NDC 0409-7248-13 [00409724813]

Hetastarch in Sodium Chloride INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberBA740193
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-07-07

NDC 0409-7248-49 [00409724849]

Hetastarch in Sodium Chloride INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberBA740193
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-02-28
Marketing End Date2018-05-01

NDC 0409-7248-59 [00409724859]

Hetastarch in Sodium Chloride INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberBA740193
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-05-26
Marketing End Date2018-05-01

Drug Details

Active Ingredients

IngredientStrength
HETASTARCH6 g/100mL

OpenFDA Data

SPL SET ID:d64f961a-3e1f-4b04-cf83-604474af2775
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310757
  • Pharmacological Class

    • Plasma Volume Expander [EPC]
    • Increased Intravascular Volume [PE]
    • Osmotic Activity [MoA]
    • Starch [CS]

    NDC Crossover Matching brand name "Hetastarch in Sodium Chloride" or generic name "Hetastarch"

    NDCBrand NameGeneric Name
    0409-7248Hetastarch in Sodium ChlorideHETASTARCH
    0264-1965HESPANHetastarch in Sodium Chloride
    0409-1555HextendHETASTARCH

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