Package 0404-9965-99

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9965-99
Digits Only 0404996599
Product NDC 0404-9965
Description

1 VIAL in 1 BAG (0404-9965-99) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-01-11
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "38ebe239-ebab-4a1a-8b1e-aad0e36915ea", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807516"], "spl_set_id": ["1bda7fa4-fdee-410a-a216-02cfbf91632f"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9965-99)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0404-9965-99", "marketing_start_date": "20220111"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "0404-9965_38ebe239-ebab-4a1a-8b1e-aad0e36915ea", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "0404-9965", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA062911", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}