NDC 17271-720

Dextrose

Dextrose Monohydrate

Dextrose 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 Dextrose Monohydrate.

Product ID17271-720_37d2886f-95ad-4b8a-a981-b7b707ffd172
NDC17271-720
Product TypeHuman Prescription Drug
Proprietary NameDextrose
Generic NameDextrose Monohydrate
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2016-10-21
Marketing CategoryANDA / ANDA
Application NumberANDA207449
Labeler NameBecton Dickinson and Company
Substance NameDEXTROSE MONOHYDRATE
Active Ingredient Strength50 mg/mL
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 17271-720-02

60 BAG in 1 CASE (17271-720-02) > 50 mL in 1 BAG
Marketing Start Date2018-07-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17271-720-06 [17271072006]

Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA207449
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-10-21
Inactivation Date2020-01-31
Reactivation Date2020-03-18

NDC 17271-720-03 [17271072003]

Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA207449
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2020-03-09
Inactivation Date2020-01-31
Reactivation Date2020-03-18

NDC 17271-720-07 [17271072007]

Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA207449
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-10-21
Inactivation Date2020-01-31
Reactivation Date2020-03-18

NDC 17271-720-02 [17271072002]

Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA207449
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-31

NDC 17271-720-05 [17271072005]

Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA207449
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-10-21
Inactivation Date2020-01-31
Reactivation Date2020-03-18

Drug Details

Active Ingredients

IngredientStrength
DEXTROSE MONOHYDRATE50 mg/mL

OpenFDA Data

SPL SET ID:c1f72bce-4bef-49db-a8da-f26a703d6748
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1795607
  • 1795610
  • 1795612
  • 1795609
  • NDC Crossover Matching brand name "Dextrose" or generic name "Dextrose Monohydrate"

    NDCBrand NameGeneric Name
    0264-1290DextroseDEXTROSE
    0264-1510DextroseDextrose
    0264-7387DextroseDextrose
    0264-7510DEXTROSEDEXTROSE
    0264-7520DEXTROSEDEXTROSE
    0338-0017DEXTROSEDEXTROSE MONOHYDRATE
    0338-0023DEXTROSEDEXTROSE MONOHYDRATE
    0338-0062DEXTROSEdextrose monohydrate
    0338-0066DEXTROSEdextrose monohydrate
    0338-0070DEXTROSEdextrose monohydrate
    0338-0074DEXTROSEdextrose monohydrate
    0409-4902DextroseDextrose
    0409-6648DextroseDextrose
    0409-7120DextroseDextrose
    0409-7100DextroseDextrose
    0409-7922DextroseDextrose
    0409-7923DextroseDextrose
    0409-7517DextroseDextrose
    0409-7918DextroseDextrose
    0409-7935DextroseDextrose
    0409-7930DextroseDextrose
    0409-7936DextroseDextrose
    0409-7937DextroseDextrose
    0409-7938DextroseDextrose
    0409-8004DextroseDextrose
    70518-1427DextroseDextrose
    71872-7003DextroseDextrose
    71872-7057DextroseDextrose
    71872-7102DextroseDextrose
    17271-720DextroseDextrose
    50090-1889DextroseDextrose
    51662-1214DEXTROSEDEXTROSE
    51662-1215DEXTROSEDEXTROSE
    51662-1306DEXTROSEDEXTROSE
    52584-517DextroseDextrose
    52584-648DextroseDextrose
    52584-902DextroseDextrose
    55154-2886DEXTROSEDEXTROSE
    55154-2887DEXTROSEDEXTROSE
    55154-2885DEXTROSEDEXTROSE
    55154-6977DextroseDextrose
    0338-0078DEXTROSEDEXTROSE
    0338-0082DEXTROSEDEXTROSE
    0338-0719DEXTROSEDEXTROSE
    0338-9147DextroseDextrose
    0338-0551DextroseDextrose
    0338-9533DextroseDextrose

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