Package 67296-2143-4

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-2143-4
Digits Only 6729621434
Product NDC 67296-2143
Description

4 BLISTER PACK in 1 CARTON (67296-2143-4) / 10 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-10-26
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4637f68c-f96e-cf38-e063-6294a90afdcf", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["313570"], "spl_set_id": ["3745b502-c222-e307-e063-6394a90a697e"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (67296-2143-4)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "67296-2143-4", "marketing_start_date": "20151026"}], "brand_name": "vancomycin hydrochloride", "product_id": "67296-2143_4637f68c-f96e-cf38-e063-6294a90afdcf", "dosage_form": "CAPSULE", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "67296-2143", "generic_name": "vancomycin hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vancomycin hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "125 mg/1"}], "application_number": "NDA050606", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20151026", "listing_expiration_date": "20261231"}