Package 69292-512-50

Brand: cefpodoxime proxetil

Generic: cefpodoxime proxetil
NDC Package

Package Facts

Identity

Package NDC 69292-512-50
Digits Only 6929251250
Product NDC 69292-512
Product ID 69292-512_849a91fa-6412-4985-a567-528c508e6815
Description

500 TABLET, FILM COATED in 1 BOTTLE (69292-512-50)

Marketing

Marketing Status
Marketed Since 2022-08-26
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": "849a91fa-6412-4985-a567-528c508e6815", "openfda": {"upc": ["0369292510506", "0369292512500"], "unii": ["2TB00A1Z7N"], "rxcui": ["309076", "309078"], "spl_set_id": ["849a91fa-6412-4985-a567-528c508e6815"], "manufacturer_name": ["Amici Pharmaceuticals, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69292-512-01)", "package_ndc": "69292-512-01", "marketing_start_date": "20220826"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69292-512-50)", "package_ndc": "69292-512-50", "marketing_start_date": "20220826"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "69292-512_849a91fa-6412-4985-a567-528c508e6815", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "69292-512", "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": "20220826", "listing_expiration_date": "20261231"}