Package 68071-3441-2

Brand: cefpodoxime proxetil

Generic: cefpodoxime proxetil
NDC Package

Package Facts

Identity

Package NDC 68071-3441-2
Digits Only 6807134412
Product NDC 68071-3441
Product ID 68071-3441_2d80b340-7ddc-adf0-e063-6294a90af485
Description

20 TABLET, FILM COATED in 1 BOTTLE (68071-3441-2)

Marketing

Marketing Status
Marketed Since 2023-06-19
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": "2d80b340-7ddc-adf0-e063-6294a90af485", "openfda": {"upc": ["0368071344127"], "unii": ["2TB00A1Z7N"], "rxcui": ["309078"], "spl_set_id": ["fe827f61-9336-72e7-e053-6394a90af75f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3441-2)", "package_ndc": "68071-3441-2", "marketing_start_date": "20230619"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "68071-3441_2d80b340-7ddc-adf0-e063-6294a90af485", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-3441", "generic_name": "Cefpodoxime Proxetil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}