Package 0781-5438-01

Brand: cefpodoxime proxetil

Generic: cefpodoxime proxetil
NDC Package

Package Facts

Identity

Package NDC 0781-5438-01
Digits Only 0781543801
Product NDC 0781-5438
Product ID 0781-5438_6878b572-5711-43a8-9972-1410927f1f14
Description

100 TABLET, FILM COATED in 1 BOTTLE (0781-5438-01)

Marketing

Marketing Status
Marketed Since 2008-05-28
Brand cefpodoxime proxetil
Generic cefpodoxime proxetil
Sample Package No

Linked Drug Pages (1)

Cefpodoxime Proxetil ndc-match (0.95)

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 (0781-5438-01)", "package_ndc": "0781-5438-01", "marketing_start_date": "20080528"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (0781-5438-20)", "package_ndc": "0781-5438-20", "marketing_start_date": "20080528"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "0781-5438_6878b572-5711-43a8-9972-1410927f1f14", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0781-5438", "generic_name": "Cefpodoxime Proxetil", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefpodoxime Proxetil", "active_ingredients": [{"name": "CEFPODOXIME PROXETIL", "strength": "100 mg/1"}], "application_number": "ANDA065462", "marketing_category": "ANDA", "marketing_start_date": "20080528", "listing_expiration_date": "20261231"}