Package 69778-931-04

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 69778-931-04
Digits Only 6977893104
Product NDC 69778-931
Product ID 69778-931_5f2379e6-9041-4de6-83a2-f63fa36db0d9
Description

500 CAPSULE in 1 BOTTLE, PLASTIC (69778-931-04)

Marketing

Marketing Status
Marketed Since 2016-10-11
Brand cephalexin
Generic cephalexin
Sample Package No

Linked Drug Pages (1)

Cephalexin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5f2379e6-9041-4de6-83a2-f63fa36db0d9", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309112", "309114"], "spl_set_id": ["bf9a6c06-11fd-4fb7-9cf5-e8e787758c1c"], "manufacturer_name": ["Pharma-C, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (69778-931-04)", "package_ndc": "69778-931-04", "marketing_start_date": "20161011"}], "brand_name": "Cephalexin", "product_id": "69778-931_5f2379e6-9041-4de6-83a2-f63fa36db0d9", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "69778-931", "generic_name": "Cephalexin", "labeler_name": "Pharma-C, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "500 mg/1"}], "application_number": "ANDA065152", "marketing_category": "ANDA", "marketing_start_date": "20101015", "listing_expiration_date": "20261231"}