cefpodoxime proxetil

Generic: cefpodoxime proxetil

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefpodoxime proxetil
Generic Name cefpodoxime proxetil
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cefpodoxime proxetil 100 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-095
Product ID 65862-095_12ee6554-adfc-4c3b-b87e-3568576359a6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065370
Listing Expiration 2026-12-31
Marketing Start 2007-06-11

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862095
Hyphenated Format 65862-095

Supplemental Identifiers

RxCUI
309076 309078
UNII
2TB00A1Z7N

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cefpodoxime proxetil (source: ndc)
Generic Name cefpodoxime proxetil (source: ndc)
Application Number ANDA065370 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (65862-095-01)
  • 20 TABLET, FILM COATED in 1 BOTTLE (65862-095-20)
  • 250 TABLET, FILM COATED in 1 BOTTLE (65862-095-25)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (65862-095-99)
source: ndc

Packages (4)

65862-095-01 100 TABLET, FILM COATED in 1 BOTTLE (65862-095-01) 65862-095-20 20 TABLET, FILM COATED in 1 BOTTLE (65862-095-20) 65862-095-25 250 TABLET, FILM COATED in 1 BOTTLE (65862-095-25) 65862-095-99 1000 TABLET, FILM COATED in 1 BOTTLE (65862-095-99)

Ingredients (1)

cefpodoxime proxetil (100 mg/1)

Linked Drug Pages (1)

CEFPODOXIME PROXETIL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "12ee6554-adfc-4c3b-b87e-3568576359a6", "openfda": {"unii": ["2TB00A1Z7N"], "rxcui": ["309076", "309078"], "spl_set_id": ["c36f2137-98bb-4583-89f7-6bce9582c465"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-095-01)", "package_ndc": "65862-095-01", "marketing_start_date": "20070611"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (65862-095-20)", "package_ndc": "65862-095-20", "marketing_start_date": "20070611"}, {"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE (65862-095-25)", "package_ndc": "65862-095-25", "marketing_start_date": "20231006"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-095-99)", "package_ndc": "65862-095-99", "marketing_start_date": "20070611"}], "brand_name": "CEFPODOXIME PROXETIL", "product_id": "65862-095_12ee6554-adfc-4c3b-b87e-3568576359a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "65862-095", "generic_name": "CEFPODOXIME PROXETIL", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFPODOXIME PROXETIL", "active_ingredients": [{"name": "CEFPODOXIME PROXETIL", "strength": "100 mg/1"}], "application_number": "ANDA065370", "marketing_category": "ANDA", "marketing_start_date": "20070611", "listing_expiration_date": "20261231"}