vancomycin hydrochloride

Generic: vancomycin hydrochloride

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vancomycin hydrochloride
Generic Name vancomycin hydrochloride
Labeler bluepoint laboratories
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vancomycin hydrochloride 10 g/1

Manufacturer
BluePoint Laboratories

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
glycopeptide antibacterial [epc] glycopeptides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001407
Hyphenated Format 68001-407

Supplemental Identifiers

RxCUI
239209 313572
UNII
71WO621TJD

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/1
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (68001-407-75) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (1)

vancomycin hydrochloride (10 g/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"}