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 10 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
55150-206
Product ID
55150-206_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
55150206
Hyphenated Format
55150-206
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
- 10 g/1
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-206-99) / 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 (55150-206-99) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "55150-206-99", "marketing_start_date": "20160329"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "55150-206_a5a491c0-5875-4031-b547-c33e02413357", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "55150-206", "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": "10 g/1"}], "application_number": "ANDA205779", "marketing_category": "ANDA", "marketing_start_date": "20160329", "listing_expiration_date": "20261231"}