vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 750 mg/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-203
Product ID
63323-203_8270ac4f-3c40-4db1-8083-bebced4fee14
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062663
Listing Expiration
2026-12-31
Marketing Start
2016-08-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323203
Hyphenated Format
63323-203
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
ANDA062663 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/15mL
Packaging
- 10 VIAL in 1 TRAY (63323-203-26) / 15 mL in 1 VIAL (63323-203-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "8270ac4f-3c40-4db1-8083-bebced4fee14", "openfda": {"upc": ["0363323203412"], "unii": ["71WO621TJD"], "rxcui": ["1807518"], "spl_set_id": ["9bfe30f8-c662-4af3-bc82-f0102eef8952"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-203-26) / 15 mL in 1 VIAL (63323-203-41)", "package_ndc": "63323-203-26", "marketing_start_date": "20160817"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63323-203_8270ac4f-3c40-4db1-8083-bebced4fee14", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "63323-203", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "750 mg/15mL"}], "application_number": "ANDA062663", "marketing_category": "ANDA", "marketing_start_date": "20160817", "listing_expiration_date": "20261231"}