vancomycin hydrochloride

Generic: vancomycin hydrochloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vancomycin hydrochloride
Generic Name vancomycin hydrochloride
Labeler hospira, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vancomycin hydrochloride 500 mg/1

Manufacturer
Hospira, Inc.

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
glycopeptide antibacterial [epc] glycopeptides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04094332
Hyphenated Format 0409-4332

Supplemental Identifiers

RxCUI
1807513 1807516 1807518 2049890
UNII
71WO621TJD

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 VIAL in 1 TRAY (0409-4332-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0409-4332-11)
source: ndc

Packages (1)

Ingredients (1)

vancomycin hydrochloride (500 mg/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"}