vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: bluepoint laboratoriesDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
bluepoint laboratories
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 10 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
68001-407
Product ID
68001-407_e94323bb-8135-b34a-e053-2995a90a7ab8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204125
Listing Expiration
2026-12-31
Marketing Start
2019-08-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68001407
Hyphenated Format
68001-407
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
ANDA204125 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 g/1
Packaging
- 1 VIAL, GLASS in 1 CARTON (68001-407-75) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e94323bb-8135-b34a-e053-2995a90a7ab8", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["f28e3c2b-ae31-4c2a-8178-53962b7b213c"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (68001-407-75) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS", "package_ndc": "68001-407-75", "marketing_start_date": "20190823"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "68001-407_e94323bb-8135-b34a-e053-2995a90a7ab8", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "68001-407", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "10 g/1"}], "application_number": "ANDA204125", "marketing_category": "ANDA", "marketing_start_date": "20190823", "listing_expiration_date": "20261231"}