Package 71335-2734-1

Brand: cephalexin

Generic: cephalexin
NDC Package

Package Facts

Identity

Package NDC 71335-2734-1
Digits Only 7133527341
Product NDC 71335-2734
Product ID 71335-2734_20b7a536-9dca-4a22-af63-ff82f1163153
Description

100 mL in 1 BOTTLE (71335-2734-1)

Marketing

Marketing Status
Marketed Since 2025-07-29
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": "20b7a536-9dca-4a22-af63-ff82f1163153", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["1bfa8744-24ee-4c70-845c-c532b8084433"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (71335-2734-1)", "package_ndc": "71335-2734-1", "marketing_start_date": "20250729"}], "brand_name": "Cephalexin", "product_id": "71335-2734_20b7a536-9dca-4a22-af63-ff82f1163153", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71335-2734", "generic_name": "Cephalexin", "labeler_name": "Bryant Ranch Prepack", "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"}