Package 72162-2305-4

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2305-4
Digits Only 7216223054
Product NDC 72162-2305
Description

50 CAPSULE in 1 BOTTLE (72162-2305-4)

Marketing

Marketing Status
Marketed Since 2024-05-13
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38c75f1c-f29c-4671-aa99-f9d3f7c650ef", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["313570"], "spl_set_id": ["d6b8147b-5f93-49ee-8b27-78fe58987c90"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE in 1 BOTTLE (72162-2305-4)", "package_ndc": "72162-2305-4", "marketing_start_date": "20240513"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "72162-2305_38c75f1c-f29c-4671-aa99-f9d3f7c650ef", "dosage_form": "CAPSULE", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "72162-2305", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "125 mg/1"}], "application_number": "ANDA210729", "marketing_category": "ANDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}