Package 67877-892-01

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 67877-892-01
Digits Only 6787789201
Product NDC 67877-892
Product ID 67877-892_779b70b9-d16c-4421-9e45-7800e947690d
Description

100 TABLET in 1 BOTTLE (67877-892-01)

Marketing

Marketing Status
Marketed Since 2024-10-21
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": "779b70b9-d16c-4421-9e45-7800e947690d", "openfda": {"upc": ["0367877892849"], "unii": ["OBN7UDS42Y"], "rxcui": ["197454", "309115"], "spl_set_id": ["36882c6d-7b6f-41e3-8c54-e3b0073b8c07"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-892-01)", "package_ndc": "67877-892-01", "marketing_start_date": "20241021"}], "brand_name": "Cephalexin", "product_id": "67877-892_779b70b9-d16c-4421-9e45-7800e947690d", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67877-892", "generic_name": "Cephalexin", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "500 mg/1"}], "application_number": "ANDA218947", "marketing_category": "ANDA", "marketing_start_date": "20241021", "listing_expiration_date": "20261231"}