Package 68071-3616-4

Brand: cefpodoxime proxetil

Generic: cefpodoxime proxetil
NDC Package

Package Facts

Identity

Package NDC 68071-3616-4
Digits Only 6807136164
Product NDC 68071-3616
Product ID 68071-3616_1b40454e-994c-39d8-e063-6394a90a97cb
Description

14 TABLET, FILM COATED in 1 BOTTLE (68071-3616-4)

Marketing

Marketing Status
Marketed Since 2024-06-19
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": "1b40454e-994c-39d8-e063-6394a90a97cb", "openfda": {"upc": ["0368071361643"], "unii": ["2TB00A1Z7N"], "rxcui": ["309076"], "spl_set_id": ["1b405104-650b-c8e3-e063-6294a90a9e8a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-3616-4)", "package_ndc": "68071-3616-4", "marketing_start_date": "20240619"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "68071-3616_1b40454e-994c-39d8-e063-6394a90a97cb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-3616", "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": "100 mg/1"}], "application_number": "ANDA210568", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}