Package 0093-2238-01

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 0093-2238-01
Digits Only 0093223801
Product NDC 0093-2238
Product ID 0093-2238_39e510b0-2478-4e34-81a1-20f002a6ae35
Description

100 TABLET in 1 BOTTLE (0093-2238-01)

Marketing

Marketing Status
Marketed Since 1990-09-30
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": "39e510b0-2478-4e34-81a1-20f002a6ae35", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["197454", "309115"], "spl_set_id": ["445b2a87-2e4f-483a-abe8-26fefd67514a"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-2238-01)", "package_ndc": "0093-2238-01", "marketing_start_date": "19900930"}], "brand_name": "Cephalexin", "product_id": "0093-2238_39e510b0-2478-4e34-81a1-20f002a6ae35", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0093-2238", "generic_name": "Cephalexin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA063024", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}