Package 70436-023-82

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70436-023-82
Digits Only 7043602382
Product NDC 70436-023
Product ID 70436-023_d1af3995-ce44-521d-e053-2a95a90ada94
Description

1 VIAL in 1 CARTON (70436-023-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-02-06
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

VANCOMYCIN HYDROCHLORIDE ndc-match (0.95)

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 (70436-023-82)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "70436-023-82", "marketing_start_date": "20210206"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "70436-023_d1af3995-ce44-521d-e053-2a95a90ada94", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "70436-023", "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": "10 g/1"}], "application_number": "ANDA215821", "marketing_category": "ANDA", "marketing_start_date": "20210206", "listing_expiration_date": "20261231"}