Package 65219-016-10

Brand: ampicillin

Generic: ampicillin sodium
NDC Package

Package Facts

Identity

Package NDC 65219-016-10
Digits Only 6521901610
Product NDC 65219-016
Description

10 VIAL in 1 CARTON (65219-016-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-016-01)

Marketing

Marketing Status
Marketed Since 2020-08-03
Brand ampicillin
Generic ampicillin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "38c6c088-e4ab-4859-b4d9-89e846cf9d5f", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721473", "1721474", "1721475", "1721476"], "spl_set_id": ["8dbb4c71-8543-08f1-e053-2995a90af88d"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (65219-016-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-016-01)", "package_ndc": "65219-016-10", "marketing_start_date": "20200803"}], "brand_name": "Ampicillin", "product_id": "65219-016_38c6c088-e4ab-4859-b4d9-89e846cf9d5f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "65219-016", "generic_name": "ampicillin sodium", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA062719", "marketing_category": "ANDA", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}