Package 71335-2948-1

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2948-1
Digits Only 7133529481
Product NDC 71335-2948
Product ID 71335-2948_bbbbe78c-d261-4630-8abb-b653a6f9a479
Description

80 mL in 1 BOTTLE (71335-2948-1)

Marketing

Marketing Status
Marketed Since 2025-11-06
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": "bbbbe78c-d261-4630-8abb-b653a6f9a479", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["2000134"], "spl_set_id": ["8193f588-a032-451e-a0a1-819a5ea834c8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "80 mL in 1 BOTTLE (71335-2948-1)", "package_ndc": "71335-2948-1", "marketing_start_date": "20251106"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "71335-2948_bbbbe78c-d261-4630-8abb-b653a6f9a479", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "71335-2948", "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/5mL"}], "application_number": "ANDA061667", "marketing_category": "ANDA", "marketing_start_date": "20190909", "listing_expiration_date": "20261231"}