vancomycin hydrochloride

Generic: vancomycin hydrochloride

Labeler: slate run pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vancomycin hydrochloride
Generic Name vancomycin hydrochloride
Labeler slate run pharmaceuticals, llc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vancomycin hydrochloride 5 g/1

Manufacturer
Slate Run Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 70436-022
Product ID 70436-022_d1af3995-ce44-521d-e053-2a95a90ada94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215821
Listing Expiration 2026-12-31
Marketing Start 2021-02-06

Pharmacologic Class

Classes
glycopeptide antibacterial [epc] glycopeptides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70436022
Hyphenated Format 70436-022

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 ANDA215821 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/1
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (70436-022-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

70436-022-82 1 VIAL in 1 CARTON (70436-022-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Ingredients (1)

vancomycin hydrochloride (5 g/1)

Linked Drug Pages (1)

VANCOMYCIN HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "d1af3995-ce44-521d-e053-2a95a90ada94", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["6ea38b4d-a6d2-4826-8110-ae42c9f7a42a"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70436-022-82)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "70436-022-82", "marketing_start_date": "20210206"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "70436-022_d1af3995-ce44-521d-e053-2a95a90ada94", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "70436-022", "generic_name": "VANCOMYCIN HYDROCHLORIDE", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VANCOMYCIN HYDROCHLORIDE", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "5 g/1"}], "application_number": "ANDA215821", "marketing_category": "ANDA", "marketing_start_date": "20210206", "listing_expiration_date": "20261231"}