vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
hospira, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0409-6534
Product ID
0409-6534_771a44e0-5858-449c-be36-438a9ff52e67
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062931
Listing Expiration
2026-12-31
Marketing Start
2005-06-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04096534
Hyphenated Format
0409-6534
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
vancomycin hydrochloride (source: ndc)
Generic Name
vancomycin hydrochloride (source: ndc)
Application Number
ANDA062931 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6534-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0409-6534-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "771a44e0-5858-449c-be36-438a9ff52e67", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807513", "1807516", "1807518"], "spl_set_id": ["2fd9de3f-a95f-451c-a687-d2e1306e53bf"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6534-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0409-6534-11)", "package_ndc": "0409-6534-01", "marketing_start_date": "20050616"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "0409-6534_771a44e0-5858-449c-be36-438a9ff52e67", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "0409-6534", "generic_name": "VANCOMYCIN HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA062931", "marketing_category": "ANDA", "marketing_start_date": "20050616", "listing_expiration_date": "20261231"}