Package 0404-9818-99
Brand: ampicillin
Generic: ampicillin sodiumPackage Facts
Identity
Package NDC
0404-9818-99
Digits Only
0404981899
Product NDC
0404-9818
Description
1 VIAL in 1 BAG (0404-9818-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Marketing
Marketing Status
Brand
ampicillin
Generic
ampicillin sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1be878fd-112e-49ad-904c-3def0847ba19", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721476"], "spl_set_id": ["06ca924c-5f3a-4924-90f4-5ba623daaa0e"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9818-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "0404-9818-99", "marketing_start_date": "20220117"}], "brand_name": "AMPICILLIN", "product_id": "0404-9818_1be878fd-112e-49ad-904c-3def0847ba19", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0404-9818", "generic_name": "AMPICILLIN SODIUM", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPICILLIN", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "2 g/1"}], "application_number": "ANDA065499", "marketing_category": "ANDA", "marketing_start_date": "20220117", "listing_expiration_date": "20261231"}