Package 25021-150-10

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-150-10
Digits Only 2502115010
Product NDC 25021-150
Description

10 VIAL in 1 CARTON (25021-150-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-07-15
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": "9421f884-7b57-4a9a-8389-a45a70dd4598", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807513", "1807516"], "spl_set_id": ["4843726f-6e79-6e20-2620-4a54616e6479"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-150-10)  / 10 mL in 1 VIAL", "package_ndc": "25021-150-10", "marketing_start_date": "20230715"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "25021-150_9421f884-7b57-4a9a-8389-a45a70dd4598", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "25021-150", "generic_name": "vancomycin hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "500 mg/10mL"}], "application_number": "ANDA205694", "marketing_category": "ANDA", "marketing_start_date": "20230715", "listing_expiration_date": "20261231"}