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 5 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-295
Product ID
63323-295_020618ad-8f1f-4189-a95c-254f05a077cc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062663
Listing Expiration
2026-12-31
Marketing Start
2001-07-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323295
Hyphenated Format
63323-295
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
- 5 g/100mL
Packaging
- 1 BOTTLE in 1 CARTON (63323-295-66) / 100 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "020618ad-8f1f-4189-a95c-254f05a077cc", "openfda": {"upc": ["0363323295660", "0363323314668"], "unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["0713a847-a334-4b73-af22-343aa06621b9"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63323-295-66) / 100 mL in 1 BOTTLE", "package_ndc": "63323-295-66", "marketing_start_date": "20010717"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63323-295_020618ad-8f1f-4189-a95c-254f05a077cc", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "63323-295", "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": "5 g/100mL"}], "application_number": "ANDA062663", "marketing_category": "ANDA", "marketing_start_date": "20010717", "listing_expiration_date": "20261231"}