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Last Updated: November 15, 2024

Details for New Drug Application (NDA): 065046


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NDA 065046 describes CEFUROXIME SODIUM, which is a drug marketed by Acs Dobfar Spa, Fresenius Kabi Usa, Hikma, Hospira Inc, Teva Pharms, Watson Labs Inc, and Samson Medcl, and is included in fourteen NDAs. It is available from two suppliers. Additional details are available on the CEFUROXIME SODIUM profile page.

The generic ingredient in CEFUROXIME SODIUM is cefuroxime sodium. There are sixty-two drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the cefuroxime sodium profile page.
Summary for 065046
Tradename:CEFUROXIME SODIUM
Applicant:Hikma
Ingredient:cefuroxime sodium
Patents:0
Pharmacology for NDA: 065046
Suppliers and Packaging for NDA: 065046
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
CEFUROXIME SODIUM cefuroxime sodium INJECTABLE;INJECTION 065046 ANDA Hikma Pharmaceuticals USA Inc. 0143-9569 0143-9569-10 10 VIAL in 1 CARTON (0143-9569-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9569-01)
CEFUROXIME SODIUM cefuroxime sodium INJECTABLE;INJECTION 065046 ANDA Hikma Pharmaceuticals USA Inc. 0143-9976 0143-9976-03 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0143-9976-03) / 82.5 mL in 1 VIAL, PHARMACY BULK PACKAGE (0143-9976-91)

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrengthEQ 7.5GM BASE/VIAL
Approval Date:Jan 9, 2004TE:RLD:No

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