Package 51662-1595-3
Brand: ampicillin
Generic: ampicillinPackage Facts
Identity
Package NDC
51662-1595-3
Digits Only
5166215953
Product NDC
51662-1595
Description
10 POUCH in 1 CASE (51662-1595-3) / 1 VIAL in 1 POUCH (51662-1595-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Marketing
Marketing Status
Brand
ampicillin
Generic
ampicillin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "100d207d-d9fb-7c75-e063-6394a90a53e8", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721473"], "spl_set_id": ["e47a21b1-bbdb-4321-e053-2a95a90a3b4a"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 POUCH in 1 CASE (51662-1595-3) / 1 VIAL in 1 POUCH (51662-1595-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "51662-1595-3", "marketing_start_date": "20220818"}], "brand_name": "AMPICILLIN", "product_id": "51662-1595_100d207d-d9fb-7c75-e063-6394a90a53e8", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "51662-1595", "generic_name": "AMPICILLIN", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPICILLIN", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA062719", "marketing_category": "ANDA", "marketing_start_date": "20220818", "listing_expiration_date": "20261231"}