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 2 g/40mL
Manufacturer
Identifiers & Regulatory
Product NDC
72078-066
Product ID
72078-066_40a88420-5fcb-4715-abc5-595a18fd08d0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA209481
Listing Expiration
2026-12-31
Marketing Start
2024-07-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72078066
Hyphenated Format
72078-066
Supplemental Identifiers
RxCUI
UPC
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
NDA209481 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 g/40mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (72078-066-99) / 50 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "40a88420-5fcb-4715-abc5-595a18fd08d0", "openfda": {"upc": ["0372078065503", "0372078066500"], "unii": ["71WO621TJD"], "rxcui": ["2688632", "2688634"], "spl_set_id": ["40a88420-5fcb-4715-abc5-595a18fd08d0"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72078-066-99) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72078-066-99", "marketing_start_date": "20240723"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "72078-066_40a88420-5fcb-4715-abc5-595a18fd08d0", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "72078-066", "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": "2 g/40mL"}], "application_number": "NDA209481", "marketing_category": "NDA", "marketing_start_date": "20240723", "listing_expiration_date": "20261231"}