Package 0404-9816-99

Brand: ampicillin

Generic: ampicillin sodium
NDC Package

Package Facts

Identity

Package NDC 0404-9816-99
Digits Only 0404981699
Product NDC 0404-9816
Description

1 VIAL in 1 BAG (0404-9816-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Discontinued 2026-04-30
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": "bd962345-a6a6-4357-829a-97945b31311f", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721475"], "spl_set_id": ["294b2a06-695d-4f51-99e4-248b772db55c"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9816-99)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "0404-9816-99", "marketing_end_date": "20260430", "marketing_start_date": "20220108"}], "brand_name": "AMPICILLIN", "product_id": "0404-9816_bd962345-a6a6-4357-829a-97945b31311f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0404-9816", "generic_name": "AMPICILLIN SODIUM", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPICILLIN", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065499", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20220108"}