cefpodoxime proxetil

Generic: cefpodoxime proxetil

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefpodoxime proxetil
Generic Name cefpodoxime proxetil
Labeler sandoz inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cefpodoxime proxetil 200 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-5439
Product ID 0781-5439_6878b572-5711-43a8-9972-1410927f1f14
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065462
Listing Expiration 2026-12-31
Marketing Start 2008-05-28

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07815439
Hyphenated Format 0781-5439

Supplemental Identifiers

RxCUI
309076 309078
UPC
0307815439019 0307815439200 0307815438203
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 ANDA065462 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0781-5439-01)
  • 20 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20)
source: ndc

Packages (2)

0781-5439-01 100 TABLET, FILM COATED in 1 BOTTLE (0781-5439-01) 0781-5439-20 20 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20)

Ingredients (1)

cefpodoxime proxetil (200 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": "6878b572-5711-43a8-9972-1410927f1f14", "openfda": {"upc": ["0307815439019", "0307815439200", "0307815438203"], "unii": ["2TB00A1Z7N"], "rxcui": ["309076", "309078"], "spl_set_id": ["8519a9d8-7106-4545-bc58-859ee9a6708e"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-5439-01)", "package_ndc": "0781-5439-01", "marketing_start_date": "20080528"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20)", "package_ndc": "0781-5439-20", "marketing_start_date": "20080528"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "0781-5439_6878b572-5711-43a8-9972-1410927f1f14", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0781-5439", "generic_name": "Cefpodoxime Proxetil", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefpodoxime Proxetil", "active_ingredients": [{"name": "CEFPODOXIME PROXETIL", "strength": "200 mg/1"}], "application_number": "ANDA065462", "marketing_category": "ANDA", "marketing_start_date": "20080528", "listing_expiration_date": "20261231"}