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NDC 64980-0403-50 Cefpodoxime Proxetil 100 mg/5mL Details
Cefpodoxime Proxetil 100 mg/5mL
Cefpodoxime Proxetil is a ORAL GRANULE, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Rising Pharma Holdings, Inc.. The primary component is CEFPODOXIME PROXETIL.
MedlinePlus Drug Summary
Cefpodoxime is used to treat certain infections caused by bacteria such as bronchitis (infection of the airway tubes leading to the lungs); pneumonia; gonorrhea (a sexually transmitted disease); and infections of the skin, ear, sinuses, throat, tonsils, and urinary tract. Cefpodoxime is in a class of medications called cephalosporin antibiotics. It works by stopping the growth of bacteria. Antibiotics such as cefpodoxime 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: 64980-0403-50Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cefpodoxime
Product Information
| NDC | 64980-0403 |
|---|---|
| Product ID | 64980-403_ab5e3ba3-8547-481f-b31b-02e87ed4c9f5 |
| Associated GPIs | 02300065101930 |
| GCN Sequence Number | 016930 |
| GCN Sequence Number Description | cefpodoxime proxetil SUSP RECON 100 MG/5ML ORAL |
| HIC3 | W1Y |
| HIC3 Description | CEPHALOSPORIN ANTIBIOTICS - 3RD GENERATION |
| GCN | 49302 |
| HICL Sequence Number | 006495 |
| HICL Sequence Number Description | CEFPODOXIME PROXETIL |
| Brand/Generic | Generic |
| Proprietary Name | Cefpodoxime Proxetil |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Cefpodoxime Proxetil |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | GRANULE, FOR SUSPENSION |
| Route | ORAL |
| Active Ingredient Strength | 100 |
| Active Ingredient Units | mg/5mL |
| Substance Name | CEFPODOXIME PROXETIL |
| Labeler Name | Rising Pharma Holdings, Inc. |
| Pharmaceutical Class | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA065409 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 64980-0403-50 (64980040350)
| NDC Package Code | 64980-403-50 |
|---|---|
| Billing NDC | 64980040350 |
| Package | 1 BOTTLE in 1 CARTON (64980-403-50) / 50 mL in 1 BOTTLE |
| Marketing Start Date | 2007-06-08 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |