Package 67877-243-50

Brand: cefprozil

Generic: cefprozil
NDC Package

Package Facts

Identity

Package NDC 67877-243-50
Digits Only 6787724350
Product NDC 67877-243
Product ID 67877-243_2e36bf51-2cc6-441a-ad40-6d752e3e4e9b
Description

50 TABLET, FILM COATED in 1 BOTTLE (67877-243-50)

Marketing

Marketing Status
Marketed Since 2025-01-20
Brand cefprozil
Generic cefprozil
Sample Package No

Linked Drug Pages (1)

Cefprozil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2e36bf51-2cc6-441a-ad40-6d752e3e4e9b", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197452", "197453"], "spl_set_id": ["dc3e9cae-6f4f-4045-a11e-2fbf7f94c3c0"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (67877-243-50)", "package_ndc": "67877-243-50", "marketing_start_date": "20250120"}], "brand_name": "Cefprozil", "product_id": "67877-243_2e36bf51-2cc6-441a-ad40-6d752e3e4e9b", "dosage_form": "TABLET, FILM COATED", "product_ndc": "67877-243", "generic_name": "Cefprozil", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefprozil", "active_ingredients": [{"name": "CEFPROZIL", "strength": "500 mg/1"}], "application_number": "ANDA090857", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}