Package 68788-8686-2

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 68788-8686-2
Digits Only 6878886862
Product NDC 68788-8686
Product ID 68788-8686_6994016d-9c09-45ad-b869-a8f62f8e0a80
Description

200 mL in 1 BOTTLE (68788-8686-2)

Marketing

Marketing Status
Marketed Since 2024-06-03
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": "6994016d-9c09-45ad-b869-a8f62f8e0a80", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["553485f8-890d-4929-a6bb-905221cf411d"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE (68788-8686-2)", "package_ndc": "68788-8686-2", "marketing_start_date": "20240603"}], "brand_name": "cephalexin", "product_id": "68788-8686_6994016d-9c09-45ad-b869-a8f62f8e0a80", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-8686", "generic_name": "Cephalexin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/5mL"}], "application_number": "ANDA065234", "marketing_category": "ANDA", "marketing_start_date": "20240603", "listing_expiration_date": "20261231"}