vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: fresenius kabi, llcDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
fresenius kabi, llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 1 g/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-284
Product ID
63323-284_23a89459-d331-4975-84fe-4bfa6ed2c24e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204107
Listing Expiration
2026-12-31
Marketing Start
2017-10-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323284
Hyphenated Format
63323-284
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
ANDA204107 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/20mL
Packaging
- 10 VIAL in 1 TRAY (63323-284-45) / 20 mL in 1 VIAL (63323-284-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (4)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "23a89459-d331-4975-84fe-4bfa6ed2c24e", "openfda": {"upc": ["0363323284411", "0363323221430"], "unii": ["71WO621TJD"], "rxcui": ["1807513", "1807516"], "spl_set_id": ["418c3c6a-d08d-448c-89c9-54e558c1ce16"], "manufacturer_name": ["Fresenius Kabi, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-284-45) / 20 mL in 1 VIAL (63323-284-41)", "package_ndc": "63323-284-45", "marketing_start_date": "20171026"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63323-284_23a89459-d331-4975-84fe-4bfa6ed2c24e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "63323-284", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Fresenius Kabi, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "1 g/20mL"}], "application_number": "ANDA204107", "marketing_category": "ANDA", "marketing_start_date": "20171026", "listing_expiration_date": "20261231"}