Package 68462-477-74

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68462-477-74
Digits Only 6846247774
Product NDC 68462-477
Product ID 68462-477_210eb04c-a542-44da-b4a3-7e243186b483
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (68462-477-74) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (68462-477-20)

Marketing

Marketing Status
Marketed Since 2025-03-21
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": "210eb04c-a542-44da-b4a3-7e243186b483", "openfda": {"upc": ["0368462478844", "0368462477748", "0368462479841"], "unii": ["71WO621TJD"], "rxcui": ["1807518", "2049888", "2049890"], "spl_set_id": ["0543b2b5-b1c7-4ad6-b38c-3be0086f0e06"], "manufacturer_name": ["GLENMARK PHARMACEUTICALS INC., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (68462-477-74)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (68462-477-20)", "package_ndc": "68462-477-74", "marketing_start_date": "20250321"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "68462-477_210eb04c-a542-44da-b4a3-7e243186b483", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "68462-477", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "GLENMARK PHARMACEUTICALS INC., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA218140", "marketing_category": "ANDA", "marketing_start_date": "20250321", "listing_expiration_date": "20261231"}