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 1 g/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-284
Product ID
63323-284_f9a5db80-2985-406e-a7b8-5593e3e8696e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062663
Listing Expiration
2026-12-31
Marketing Start
2000-09-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323284
Hyphenated Format
63323-284
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
ANDA062663 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/20mL
Packaging
- 10 VIAL in 1 TRAY (63323-284-21) / 20 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (4)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f9a5db80-2985-406e-a7b8-5593e3e8696e", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807513"], "spl_set_id": ["83ea3faf-fedd-4725-911f-d71a23ec5d5e"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-284-21) / 20 mL in 1 VIAL", "package_ndc": "63323-284-21", "marketing_start_date": "20000920"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "63323-284_f9a5db80-2985-406e-a7b8-5593e3e8696e", "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 USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VANCOMYCIN HYDROCHLORIDE", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "1 g/20mL"}], "application_number": "ANDA062663", "marketing_category": "ANDA", "marketing_start_date": "20000920", "listing_expiration_date": "20261231"}