NDC 0409-6664

Sodium Lactate

Sodium Lactate

Sodium Lactate 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 Lactate.

Product ID0409-6664_37def875-6c99-449f-8883-2d4a8004f030
NDC0409-6664
Product TypeHuman Prescription Drug
Proprietary NameSodium Lactate
Generic NameSodium Lactate
Dosage FormInjection, Solution, Concentrate
Route of AdministrationINTRAVENOUS
Marketing Start Date2006-06-28
Marketing CategoryNDA / NDA
Application NumberNDA018947
Labeler NameHospira, Inc.
Substance NameSODIUM LACTATE
Active Ingredient Strength6 g/10mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0409-6664-02

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6664-02) > 10 mL in 1 VIAL, SINGLE-DOSE (0409-6664-11)
Marketing Start Date2006-06-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0409-6664-02 [00409666402]

Sodium Lactate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018947
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-06-28
Marketing End Date2019-10-01

NDC 0409-6664-11 [00409666411]

Sodium Lactate INJECTION, SOLUTION, CONCENTRATE
Marketing CategoryNDA
Application NumberNDA018947
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2018-04-09
Marketing End Date2019-10-01

Drug Details

Active Ingredients

IngredientStrength
SODIUM LACTATE5.6 g/10mL

OpenFDA Data

SPL SET ID:82428c00-d0da-44e4-4884-a735c150c067
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 237378
    • © 2026 FDA.report
    This site is not affiliated with or endorsed by the FDA.