vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: samson medical technologies llcDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
samson medical technologies llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 100 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
66288-7100
Product ID
66288-7100_d607785f-563a-4816-83c4-dfc38bbc29bd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091532
Listing Expiration
2026-12-31
Marketing Start
2016-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
662887100
Hyphenated Format
66288-7100
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
ANDA091532 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 g/1
Packaging
- 1 BAG in 1 BAG (66288-7100-1) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d607785f-563a-4816-83c4-dfc38bbc29bd", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209"], "spl_set_id": ["93589e71-3a11-4797-9176-8abdb7674a87"], "manufacturer_name": ["SAMSON MEDICAL TECHNOLOGIES LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 BAG (66288-7100-1) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 BAG", "package_ndc": "66288-7100-1", "marketing_start_date": "20160601"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "66288-7100_d607785f-563a-4816-83c4-dfc38bbc29bd", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "66288-7100", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "SAMSON MEDICAL TECHNOLOGIES LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "100 g/1"}], "application_number": "ANDA091532", "marketing_category": "ANDA", "marketing_start_date": "20160601", "listing_expiration_date": "20261231"}