NDC 0143-9878

Cefoxitin

Cefoxitin

Cefoxitin is a Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by West-ward Pharmaceuticals Corp. The primary component is Cefoxitin Sodium.

Product ID0143-9878_b27301e3-bd54-4e4f-a8a4-e9842a22136b
NDC0143-9878
Product TypeHuman Prescription Drug
Proprietary NameCefoxitin
Generic NameCefoxitin
Dosage FormInjection, Powder, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2010-03-12
Marketing CategoryANDA / ANDA
Application NumberANDA065238
Labeler NameWest-Ward Pharmaceuticals Corp
Substance NameCEFOXITIN SODIUM
Active Ingredient Strength1 g/1
Pharm ClassesCephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0143-9878-25

25 VIAL in 1 CARTON (0143-9878-25) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)
Marketing Start Date2010-03-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0143-9878-25 [00143987825]

Cefoxitin INJECTION, POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA065238
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-12

NDC 0143-9878-01 [00143987801]

Cefoxitin INJECTION, POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA065238
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-02-19

Drug Details

Active Ingredients

IngredientStrength
CEFOXITIN SODIUM1 g/1

OpenFDA Data

SPL SET ID:d2c449b9-5624-4166-95b1-d7813b3d0445
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1665107
  • 1665102

    • Pharmacological Class

    • Cephalosporin Antibacterial [EPC]
    • Cephalosporins [CS]
    • Cephalosporin Antibacterial [EPC]
    • Cephalosporins [CS]

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

    NDCBrand NameGeneric Name
    0143-9876CefoxitinCefoxitin
    0143-9877CefoxitinCefoxitin
    0143-9878CefoxitinCefoxitin
    25021-109Cefoxitincefoxitin
    25021-110Cefoxitincefoxitin
    25021-111Cefoxitincefoxitin
    44567-245CefoxitinCefoxitin
    44567-246CefoxitinCefoxitin
    44567-247CefoxitinCefoxitin
    60505-0759CefoxitinCEFOXITIN
    60505-0760CefoxitinCEFOXITIN
    60505-0761CefoxitinCEFOXITIN
    63323-341CefoxitinCefoxitin Sodium
    63323-342CefoxitinCefoxitin Sodium
    63323-343CefoxitinCefoxitin
    66288-4100CefoxitinCefoxitin
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.