vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: mylan institutional llcDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
mylan institutional llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 10 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
67457-342
Product ID
67457-342_c0b65e4b-6d28-4aa1-94f5-8f26888355b1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091554
Listing Expiration
2026-12-31
Marketing Start
2013-12-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67457342
Hyphenated Format
67457-342
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
ANDA091554 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 g/100mL
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (67457-342-10) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c0b65e4b-6d28-4aa1-94f5-8f26888355b1", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209"], "spl_set_id": ["ce139a51-0471-4c31-b456-2f889f18dd2b"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (67457-342-10) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "67457-342-10", "marketing_start_date": "20131205"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "67457-342_c0b65e4b-6d28-4aa1-94f5-8f26888355b1", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "67457-342", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "10 g/100mL"}], "application_number": "ANDA091554", "marketing_category": "ANDA", "marketing_start_date": "20131205", "listing_expiration_date": "20261231"}