Package 67877-879-01

Brand: cefpodoxime proxetil

Generic: cefpodoxime proxetil
NDC Package

Package Facts

Identity

Package NDC 67877-879-01
Digits Only 6787787901
Product NDC 67877-879
Description

100 TABLET, FILM COATED in 1 BOTTLE (67877-879-01)

Marketing

Marketing Status
Marketed Since 2023-03-01
Brand cefpodoxime proxetil
Generic cefpodoxime proxetil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a9e47ee-3f6f-4be0-9b06-9430d2a5f1bd", "openfda": {"upc": ["0367877878201", "0367877879208"], "unii": ["2TB00A1Z7N"], "rxcui": ["309076", "309078"], "spl_set_id": ["ce5646cb-a450-4c2c-8499-6ecf71b12b0e"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (67877-879-01)", "package_ndc": "67877-879-01", "marketing_start_date": "20230301"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-879-05)", "package_ndc": "67877-879-05", "marketing_start_date": "20230301"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (67877-879-20)", "package_ndc": "67877-879-20", "marketing_start_date": "20230213"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "67877-879_1a9e47ee-3f6f-4be0-9b06-9430d2a5f1bd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67877-879", "generic_name": "Cefpodoxime Proxetil", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefpodoxime Proxetil", "active_ingredients": [{"name": "CEFPODOXIME PROXETIL", "strength": "200 mg/1"}], "application_number": "ANDA210568", "marketing_category": "ANDA", "marketing_start_date": "20230213", "listing_expiration_date": "20261231"}