Package 0143-9356-25

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9356-25
Digits Only 0143935625
Product NDC 0143-9356
Product ID 0143-9356_431d7445-e798-40a7-a8aa-6a8b1ac5813f
Description

25 VIAL in 1 CARTON (0143-9356-25) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9356-01)

Marketing

Marketing Status
Marketed Since 2020-08-11
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": "431d7445-e798-40a7-a8aa-6a8b1ac5813f", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807513", "1807516"], "spl_set_id": ["2f5d3131-8ddc-43a5-91f7-947c531796e7"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9356-25)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9356-01)", "package_ndc": "0143-9356-25", "marketing_start_date": "20200811"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "0143-9356_431d7445-e798-40a7-a8aa-6a8b1ac5813f", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "0143-9356", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203300", "marketing_category": "ANDA", "marketing_start_date": "20200811", "listing_expiration_date": "20261231"}