Package 68788-9539-2

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 68788-9539-2
Digits Only 6878895392
Product NDC 68788-9539
Description

200 mL in 1 BOTTLE (68788-9539-2)

Marketing

Marketing Status
Marketed Since 2013-12-03
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": "ca2da054-e63c-4dca-9f87-c4a409036430", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309110", "309113"], "spl_set_id": ["07631a8b-eb84-46aa-844e-e93e548cb9b2"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-9539-1)", "package_ndc": "68788-9539-1", "marketing_start_date": "20131203"}, {"sample": false, "description": "200 mL in 1 BOTTLE (68788-9539-2)", "package_ndc": "68788-9539-2", "marketing_start_date": "20131203"}], "brand_name": "Cephalexin", "product_id": "68788-9539_ca2da054-e63c-4dca-9f87-c4a409036430", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-9539", "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": "ANDA062703", "marketing_category": "ANDA", "marketing_start_date": "20131203", "listing_expiration_date": "20261231"}