Package 72162-2306-4

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2306-4
Digits Only 7216223064
Product NDC 72162-2306
Product ID 72162-2306_91d9dc98-b742-4507-aea8-988c8bf4e6b3
Description

50 CAPSULE in 1 BOTTLE (72162-2306-4)

Marketing

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

Linked Drug Pages (1)

Vancomycin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "91d9dc98-b742-4507-aea8-988c8bf4e6b3", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["313571"], "spl_set_id": ["7bbd2c81-33d9-4397-8795-8b9fa28cb5cf"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE in 1 BOTTLE (72162-2306-4)", "package_ndc": "72162-2306-4", "marketing_start_date": "20240513"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "72162-2306_91d9dc98-b742-4507-aea8-988c8bf4e6b3", "dosage_form": "CAPSULE", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "72162-2306", "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": "250 mg/1"}], "application_number": "ANDA210729", "marketing_category": "ANDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}