NDC 17271-703

3% Sodium Chloride

3% Sodium Chloride

3% Sodium Chloride is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Becton Dickinson And Company. The primary component is Sodium Chloride.

Product ID17271-703_ab3d79da-7b4a-4224-b0e4-46bd00bf6444
NDC17271-703
Product TypeHuman Prescription Drug
Proprietary Name3% Sodium Chloride
Generic Name3% Sodium Chloride
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2020-02-28
Marketing CategoryANDA / ANDA
Application NumberANDA209476
Labeler NameBecton Dickinson and Company
Substance NameSODIUM CHLORIDE
Active Ingredient Strength3 g/100mL
Pharm ClassesOsmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 17271-703-06

20 BAG in 1 CASE (17271-703-06) > 500 mL in 1 BAG
Marketing Start Date2020-02-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17271-703-06 [17271070306]

3% Sodium Chloride INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA209476
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-02-28

Drug Details

Active Ingredients

IngredientStrength
SODIUM CHLORIDE3 g/100mL

OpenFDA Data

SPL SET ID:a8058593-48af-457a-b0f0-166935c7d10c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 730781
  • Pharmacological Class

    • Osmotic Laxative [EPC]
    • Increased Large Intestinal Motility [PE]
    • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
    • Osmotic Activity [MoA]

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