NDC 44567-712

Cefuroxime

Cefuroxime

Cefuroxime is a Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Wg Critical Care, Llc. The primary component is Cefuroxime Sodium.

Product ID44567-712_e4a6cecb-b7bd-4e27-9535-4ab73c2ccc00
NDC44567-712
Product TypeHuman Prescription Drug
Proprietary NameCefuroxime
Generic NameCefuroxime
Dosage FormInjection, Powder, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2012-10-04
Marketing CategoryANDA / ANDA
Application NumberANDA064124
Labeler NameWG Critical Care, LLC
Substance NameCEFUROXIME SODIUM
Active Ingredient Strength8 g/80mL
Pharm ClassesCephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 44567-712-10

10 VIAL in 1 CARTON (44567-712-10) > 80 mL in 1 VIAL
Marketing Start Date2012-10-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 44567-712-10 [44567071210]

Cefuroxime INJECTION, POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA064124
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-10-04
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
CEFUROXIME SODIUM7.5 g/80mL

OpenFDA Data

SPL SET ID:a7b50175-e978-4edd-9d61-593df4806657
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 309101
  • Pharmacological Class

    • Cephalosporin Antibacterial [EPC]
    • Cephalosporins [CS]

    NDC Crossover Matching brand name "Cefuroxime" or generic name "Cefuroxime"

    NDCBrand NameGeneric Name
    0143-9567CefuroximeCefuroxime
    0143-9568CefuroximeCefuroxime
    0143-9569CefuroximeCefuroxime
    0143-9976CefuroximeCefuroxime
    0143-9977CefuroximeCefuroxime
    0143-9979CefuroximeCefuroxime
    44567-710CefuroximeCefuroxime
    44567-711CefuroximeCefuroxime
    44567-712CefuroximeCefuroxime
    44567-720CefuroximeCefuroxime
    44567-722CefuroximeCefuroxime

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