Package 71335-2950-1

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2950-1
Digits Only 7133529501
Product NDC 71335-2950
Product ID 71335-2950_81d0a232-e627-43ca-aa4d-f200ae6ef63d
Description

150 mL in 1 BOTTLE (71335-2950-1)

Marketing

Marketing Status
Marketed Since 2025-11-05
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": "81d0a232-e627-43ca-aa4d-f200ae6ef63d", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["2000134"], "spl_set_id": ["6c74b360-022a-4c4d-9e4b-0988219a78fb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (71335-2950-1)", "package_ndc": "71335-2950-1", "marketing_start_date": "20251105"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "71335-2950_81d0a232-e627-43ca-aa4d-f200ae6ef63d", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "71335-2950", "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"}