Search by Drug Name or NDC
NDC 68180-0202-05 SUPRAX 100 mg/5mL Details
SUPRAX 100 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: 68180-0202-05Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cefixime
Product Information
| NDC | 68180-0202 |
|---|---|
| Product ID | 68180-202_a71c02a7-148f-42cb-b323-34c7bcfb0bec |
| Associated GPIs | 02300060001910 |
| GCN Sequence Number | 009182 |
| GCN Sequence Number Description | cefixime SUSP RECON 100 MG/5ML ORAL |
| HIC3 | W1Y |
| HIC3 Description | CEPHALOSPORIN ANTIBIOTICS - 3RD GENERATION |
| GCN | 33120 |
| 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 | 100 |
| 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 | ANDA065129 |
| Listing Certified Through | 2022-12-31 |
Package
NDC 68180-0202-05 (68180020205)
| NDC Package Code | 68180-202-05 |
|---|---|
| Billing NDC | 68180020205 |
| Package | 6 BOTTLE in 1 CARTON (68180-202-05) / 10 mL in 1 BOTTLE (68180-202-04) |
| Marketing Start Date | 2004-03-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |