Package 25021-158-99

Brand: vancomycin

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-158-99
Digits Only 2502115899
Product NDC 25021-158
Description

1 BOTTLE in 1 CARTON (25021-158-99) / 100 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2012-09-20
Brand vancomycin
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9b6f6171-cd0c-4468-a018-ebec650749ab", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["06dcfd36-942f-4752-86ad-4c5a6fc3e48f"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (25021-158-99)  / 100 mL in 1 BOTTLE", "package_ndc": "25021-158-99", "marketing_start_date": "20120920"}], "brand_name": "Vancomycin", "product_id": "25021-158_9b6f6171-cd0c-4468-a018-ebec650749ab", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "25021-158", "generic_name": "vancomycin hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "10 g/100mL"}], "application_number": "ANDA200837", "marketing_category": "ANDA", "marketing_start_date": "20120920", "listing_expiration_date": "20261231"}