vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
eugia us llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 5 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
55150-205
Product ID
55150-205_a5a491c0-5875-4031-b547-c33e02413357
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205779
Listing Expiration
2026-12-31
Marketing Start
2016-03-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150205
Hyphenated Format
55150-205
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
ANDA205779 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 g/1
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-205-99) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a5a491c0-5875-4031-b547-c33e02413357", "openfda": {"upc": ["0355150206995", "0355150205998"], "unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["4a80cb3f-7410-47aa-af1f-ff83d1b35c55"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-205-99) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "55150-205-99", "marketing_start_date": "20160329"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "55150-205_a5a491c0-5875-4031-b547-c33e02413357", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "55150-205", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "5 g/1"}], "application_number": "ANDA205779", "marketing_category": "ANDA", "marketing_start_date": "20160329", "listing_expiration_date": "20261231"}