Package 69292-516-01
Brand: cefpodoxime proxetil
Generic: cefpodoxime proxetilPackage Facts
Identity
Package NDC
69292-516-01
Digits Only
6929251601
Product NDC
69292-516
Description
100 TABLET, FILM COATED in 1 BOTTLE (69292-516-01)
Marketing
Marketing Status
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": "157c18ee-7809-4e05-8caa-0359ef50142e", "openfda": {"unii": ["2TB00A1Z7N"], "rxcui": ["309076", "309078"], "spl_set_id": ["9d6d7f50-9838-47e3-8214-53e2dbeeadea"], "manufacturer_name": ["Amici Pharmaceuticals, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69292-516-01)", "package_ndc": "69292-516-01", "marketing_start_date": "20221221"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69292-516-50)", "package_ndc": "69292-516-50", "marketing_start_date": "20221221"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "69292-516_157c18ee-7809-4e05-8caa-0359ef50142e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "69292-516", "generic_name": "Cefpodoxime Proxetil", "labeler_name": "Amici Pharmaceuticals, 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": "20221221", "listing_expiration_date": "20261231"}