Package 63629-1970-1

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1970-1
Digits Only 6362919701
Product NDC 63629-1970
Description

80 mL in 1 BOTTLE (63629-1970-1)

Marketing

Marketing Status
Marketed Since 2019-09-09
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c47f33a-d207-4eab-a67a-a1d99c1e9502", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["2000134"], "spl_set_id": ["786bde33-9aec-4b4d-ba46-90bfd61956d0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "80 mL in 1 BOTTLE (63629-1970-1)", "package_ndc": "63629-1970-1", "marketing_start_date": "20190909"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63629-1970_4c47f33a-d207-4eab-a67a-a1d99c1e9502", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "63629-1970", "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"}