vancomycin hydrochloride

Generic: vancomycin hydrochloride

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

Drug Facts

Product Profile

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

vancomycin hydrochloride 500 mg/1

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9965
Product ID 0404-9965_38ebe239-ebab-4a1a-8b1e-aad0e36915ea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062911
Listing Expiration 2026-12-31
Marketing Start 2022-01-11

Pharmacologic Class

Classes
glycopeptide antibacterial [epc] glycopeptides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049965
Hyphenated Format 0404-9965

Supplemental Identifiers

RxCUI
1807516
UNII
71WO621TJD

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
  • 1 VIAL in 1 BAG (0404-9965-99) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

vancomycin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "38ebe239-ebab-4a1a-8b1e-aad0e36915ea", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807516"], "spl_set_id": ["1bda7fa4-fdee-410a-a216-02cfbf91632f"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9965-99)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0404-9965-99", "marketing_start_date": "20220111"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "0404-9965_38ebe239-ebab-4a1a-8b1e-aad0e36915ea", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "0404-9965", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Henry Schein, 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": "20220111", "listing_expiration_date": "20261231"}