Package 71335-2864-1

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 71335-2864-1
Digits Only 7133528641
Product NDC 71335-2864
Description

100 CAPSULE in 1 BOTTLE (71335-2864-1)

Marketing

Marketing Status
Marketed Since 2025-11-07
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": "a4c60909-548d-403a-a4b0-2ffd3c923248", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309112"], "spl_set_id": ["0384c418-b4d4-4c06-9ed9-13e864b1980b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-2864-1)", "package_ndc": "71335-2864-1", "marketing_start_date": "20251107"}], "brand_name": "Cephalexin", "product_id": "71335-2864_a4c60909-548d-403a-a4b0-2ffd3c923248", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71335-2864", "generic_name": "Cephalexin", "labeler_name": "Bryant Ranch Prepack", "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"}