Package 0338-3580-48

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0338-3580-48
Digits Only 0338358048
Product NDC 0338-3580
Description

200 mL in 1 BAG (0338-3580-48)

Marketing

Marketing Status
Marketed Since 1958-11-14
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": "db8b59dd-edfd-4c37-b875-7e73f1f0bf35", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807508", "1807510", "1807511", "2118448", "2387078"], "spl_set_id": ["99e523d8-9bde-43cb-8434-497015e5dcbd"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BAG (0338-3580-48)", "package_ndc": "0338-3580-48", "marketing_start_date": "19581114"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "0338-3580_db8b59dd-edfd-4c37-b875-7e73f1f0bf35", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "0338-3580", "generic_name": "VANCOMYCIN HYDROCHLORIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VANCOMYCIN HYDROCHLORIDE", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "750 mg/150mL"}], "application_number": "NDA050671", "marketing_category": "NDA", "marketing_start_date": "19581114", "listing_expiration_date": "20261231"}