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
0409-4332
Product ID
0409-4332_6b13ef5a-c456-4bcf-a9ec-ddc91bbd809a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062911
Listing Expiration
2026-12-31
Marketing Start
2005-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04094332
Hyphenated Format
0409-4332
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
ANDA062911 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 10 VIAL in 1 TRAY (0409-4332-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0409-4332-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6b13ef5a-c456-4bcf-a9ec-ddc91bbd809a", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807513", "1807516", "1807518", "2049890"], "spl_set_id": ["f2901045-904f-47bd-74a1-c561facd7f25"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (0409-4332-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0409-4332-11)", "package_ndc": "0409-4332-01", "marketing_start_date": "20050430"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "0409-4332_6b13ef5a-c456-4bcf-a9ec-ddc91bbd809a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "0409-4332", "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": "ANDA062911", "marketing_category": "ANDA", "marketing_start_date": "20050430", "listing_expiration_date": "20261231"}