NDC 0409-3299

Sodium Acetate

Sodium Acetate

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

Product ID0409-3299_32fac08e-7507-4e6c-b362-dc0f77f91d00
NDC0409-3299
Product TypeHuman Prescription Drug
Proprietary NameSodium Acetate
Generic NameSodium Acetate
Dosage FormInjection, Solution, Concentrate
Route of AdministrationINTRAVENOUS
Marketing Start Date2013-11-19
Marketing CategoryNDA / NDA
Application NumberNDA018893
Labeler NameHospira, Inc.
Substance NameSODIUM ACETATE ANHYDROUS
Active Ingredient Strength164 mg/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0409-3299-25

25 VIAL in 1 CASE (0409-3299-25) > 100 mL in 1 VIAL (0409-3299-45)
Marketing Start Date2013-11-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0409-3299-26 [00409329926]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-04-30

NDC 0409-3299-45 [00409329945]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-12-05

NDC 0409-3299-16 [00409329916]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-04-06

NDC 0409-3299-15 [00409329915]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-04-06

NDC 0409-3299-05 [00409329905]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-05-16

NDC 0409-3299-46 [00409329946]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-12-05

NDC 0409-3299-25 [00409329925]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-04-30

NDC 0409-3299-06 [00409329906]

Sodium Acetate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-04-30

Drug Details

Active Ingredients

IngredientStrength
SODIUM ACETATE ANHYDROUS164 mg/mL

OpenFDA Data

SPL SET ID:abc41ed1-9512-4bea-9295-1a9ca134b6c2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 237371
  • NDC Crossover Matching brand name "Sodium Acetate" or generic name "Sodium Acetate"

    NDCBrand NameGeneric Name
    0409-3299Sodium Acetatesodium acetate
    0409-7299Sodium AcetateSODIUM ACETATE
    51754-9995Sodium AcetateSodium Acetate
    63323-032SODIUM ACETATESODIUM ACETATE
    69784-230SODIUM ACETATESODIUM ACETATE
    69784-231SODIUM ACETATESODIUM ACETATE
    0517-5023Sodum AcetateSodium Acetate

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