NDC 0264-3125

Cefoxitin and Dextrose

Cefoxitin Sodium

Cefoxitin and Dextrose 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 Cefoxitin Sodium.

Product ID0264-3125_0cca0e6a-3047-4142-af33-d9b98efe85b1
NDC0264-3125
Product TypeHuman Prescription Drug
Proprietary NameCefoxitin and Dextrose
Generic NameCefoxitin Sodium
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2006-03-10
Marketing CategoryNDA / NDA
Application NumberNDA065214
Labeler NameB. Braun Medical Inc.
Substance NameCEFOXITIN SODIUM
Active Ingredient Strength2 g/50mL
Pharm ClassesCephalosporin Antibacterial [EPC], Cephalosporins [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0264-3125-11

24 CONTAINER in 1 CASE (0264-3125-11) > 50 mL in 1 CONTAINER
Marketing Start Date2006-03-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0264-3125-11 [00264312511]

Cefoxitin and Dextrose INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA065214
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-03-10

Drug Details

Active Ingredients

IngredientStrength
CEFOXITIN SODIUM2 g/50mL

OpenFDA Data

SPL SET ID:6c7e9485-1ede-411c-8c46-911439332864
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1665107
  • 1665102
  • Pharmacological Class

    • Cephalosporin Antibacterial [EPC]
    • Cephalosporins [CS]

    NDC Crossover Matching brand name "Cefoxitin and Dextrose" or generic name "Cefoxitin Sodium"

    NDCBrand NameGeneric Name
    0264-3123Cefoxitin and DextroseCEFOXITIN SODIUM
    0264-3125Cefoxitin and DextroseCEFOXITIN SODIUM
    63323-341CefoxitinCefoxitin Sodium
    63323-342CefoxitinCefoxitin Sodium

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