NDC 0264-7751

Dextrose in Lactated Ringers

Dextrose, Sodium Chloride, Sodium Lactate, Potassium Chloride, And Calcium Chloride

Dextrose in Lactated Ringers is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by B. Braun Medical Inc.. The primary component is Dextrose Monohydrate; Sodium Chloride; Sodium Lactate; Potassium Chloride; Calcium Chloride.

Product ID0264-7751_04ccd86f-4475-4210-afe0-4fff11e7f49e
NDC0264-7751
Product TypeHuman Prescription Drug
Proprietary NameDextrose in Lactated Ringers
Generic NameDextrose, Sodium Chloride, Sodium Lactate, Potassium Chloride, And Calcium Chloride
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date1988-02-24
Marketing CategoryNDA / NDA
Application NumberNDA019634
Labeler NameB. Braun Medical Inc.
Substance NameDEXTROSE MONOHYDRATE; SODIUM CHLORIDE; SODIUM LACTATE; POTASSIUM CHLORIDE; CALCIUM CHLORIDE
Active Ingredient Strength5 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
Pharm ClassesOsmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0264-7751-00

12 CONTAINER in 1 CASE (0264-7751-00) > 1000 mL in 1 CONTAINER
Marketing Start Date1988-02-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0264-7751-00 [00264775100]

Dextrose in Lactated Ringers INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA019634
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1988-02-24

NDC 0264-7751-10 [00264775110]

Dextrose in Lactated Ringers INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA019634
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1988-02-24

Drug Details

Active Ingredients

IngredientStrength
DEXTROSE MONOHYDRATE5 g/100mL

OpenFDA Data

SPL SET ID:190da07e-a616-46e6-b4e5-1c0ba39306e5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 847627
  • Pharmacological Class

    • Osmotic Laxative [EPC]
    • Increased Large Intestinal Motility [PE]
    • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
    • Osmotic Activity [MoA]
    • Potassium Compounds [CS]
    • Potassium Salt [EPC]
    • Osmotic Laxative [EPC]
    • Increased Large Intestinal Motility [PE]
    • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
    • Osmotic Activity [MoA]
    • Blood Coagulation Factor [EPC]
    • Increased Coagulation Factor Activity [PE]
    • Calcium [CS]
    • Cations
    • Divalent [CS]
    • Osmotic Laxative [EPC]
    • Increased Large Intestinal Motility [PE]
    • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
    • Osmotic Activity [MoA]
    • Potassium Compounds [CS]
    • Potassium Salt [EPC]
    • Osmotic Laxative [EPC]
    • Increased Large Intestinal Motility [PE]
    • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
    • Osmotic Activity [MoA]
    • Blood Coagulation Factor [EPC]
    • Increased Coagulation Factor Activity [PE]
    • Calcium [CS]
    • Cations
    • Divalent [CS]

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