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NDC 27437-0206-05 SUPRAX 200 mg/5mL Details

SUPRAX 200 mg/5mL

SUPRAX is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is CEFIXIME.

MedlinePlus Drug Summary

Cefixime is used to treat certain infections caused by bacteria such as bronchitis (infection of the airway tubes leading to the lungs); gonorrhea (a sexually transmitted disease); and infections of the ears, throat, tonsils, and urinary tract. Cefixime is in a class of medications called cephalosporin antibiotics. It works by killing bacteria. Antibiotics such as cefixime will not work for colds, flu, or other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.

Related Packages: 27437-0206-05
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Cefixime

Product Information

NDC	27437-0206
Product ID	27437-206_ddcc8926-f489-4ea1-93eb-e959ea8f2e1f
Associated GPIs	02300060001920
GCN Sequence Number	044428
GCN Sequence Number Description	cefixime SUSP RECON 200 MG/5ML ORAL
HIC3	W1Y
HIC3 Description	CEPHALOSPORIN ANTIBIOTICS - 3RD GENERATION
GCN	92368
HICL Sequence Number	003999
HICL Sequence Number Description	CEFIXIME
Brand/Generic	Brand
Proprietary Name	SUPRAX
Proprietary Name Suffix	n/a
Non-Proprietary Name	cefixime
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	POWDER, FOR SUSPENSION
Route	ORAL
Active Ingredient Strength	200
Active Ingredient Units	mg/5mL
Substance Name	CEFIXIME
Labeler Name	Lupin Pharmaceuticals, Inc.
Pharmaceutical Class	Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA065355
Listing Certified Through	2024-12-31

Package

NDC 27437-0206-05 (27437020605)

Pricing Information	N/A
NDC Package Code	27437-206-05
Billing NDC	27437020605
Package	25 mL in 1 BOTTLE (27437-206-05)
Marketing Start Date	2007-06-01
NDC Exclude Flag	N