Package 76420-034-40

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 76420-034-40
Digits Only 7642003440
Product NDC 76420-034
Description

40 CAPSULE in 1 BOTTLE (76420-034-40)

Marketing

Marketing Status
Marketed Since 2022-07-20
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": "e436e361-d938-7d6d-e053-2995a90a10e4", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309112"], "spl_set_id": ["891b8c0e-dbf4-4b0e-ba3f-c4c49d51510d"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "40 CAPSULE in 1 BOTTLE (76420-034-40)", "package_ndc": "76420-034-40", "marketing_start_date": "20220720"}], "brand_name": "Cephalexin", "product_id": "76420-034_e436e361-d938-7d6d-e053-2995a90a10e4", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "76420-034", "generic_name": "Cephalexin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA090836", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}