Package 68788-7529-1

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 68788-7529-1
Digits Only 6878875291
Product NDC 68788-7529
Description

100 mL in 1 BOTTLE (68788-7529-1)

Marketing

Marketing Status
Marketed Since 2019-10-04
Brand cephalexin
Generic cephalexin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f170357f-5fe8-4ad4-983a-5e46245070cb", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["6c7bfa58-2d38-4607-8c33-485ba4931c68"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-7529-1)", "package_ndc": "68788-7529-1", "marketing_start_date": "20191004"}, {"sample": false, "description": "200 mL in 1 BOTTLE (68788-7529-2)", "package_ndc": "68788-7529-2", "marketing_start_date": "20191004"}], "brand_name": "Cephalexin", "product_id": "68788-7529_f170357f-5fe8-4ad4-983a-5e46245070cb", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-7529", "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": "ANDA210221", "marketing_category": "ANDA", "marketing_start_date": "20190328", "listing_expiration_date": "20261231"}